cat. no. E0240
Ultra-pure, sterile 0.5 M EDTA solution, pH 8.0 (Na2EDTA · 2H2O dissolved in ultrapure, deionized water) for biochemistry and molecular biology applications where the presence of a divalent metal ion chelator is required. Nuclease free.
cat. no. E0270
cat. no. E0271
cat. no. E0272
cat. no. E0273
cat. no. E0274
cat. no. E0281
PBS is a sterile, isotonic saline solution. Contains calcium and magnesium. Calcium and magnesium facilitate cell binding and clumping. PBS is used for the handling, diluting and culturing of mammalian cells. It serves as an isotonic buffer for washing cells and tissues.
cat. no. E0282
PBS is a sterile, isotonic saline solution, without calcium chloride and magnesium chloride. It is used for the handling and culturing of mammalian cells. Calcium and magnesium facilitate cell binding and clumping. PBS without these ions can be used to wash and rinse suspended cells.
cat. no. E0250
TE buffer is commonly used buffer solution in molecular biology, especially in procedures involving DNA or RNA. The purpose of TE buffer is to solubilize DNA or RNA, while protecting it from degradation.
cat. no. E0503
Ready to use deoxyribonucleotides mixture. The concentration of each deoxyribonucleotide is 10 mM. Free of contaminants. The mixture is ready for use in PCR, TdT, sequencing, end-filling, nick translation and cDNA synthesis.
cat. no. E0501
Ultrapure set of dNTPs contains four separate solutions of dATP, dCTP, dGTP and dTTP supplied as aqueous solutions. dATP 2’-Deoxyadenosine 5’-triphosphate, sodium salt Molecular formula: C10H13N5O12P3 (Anion) Molecular weight: 488.16 (Anion) dCTP 2’-Deoxycytidine 5’-triphosphate, sodium salt Molecular formula: C9H13N3O13P3 (Anion) Molecular weight: 464.13 (Anion) dGTP 2’-Deoxyguanosine 5’-triphosphate, sodium salt Molecular formula: C10H13N5O13P3 (Anion) Molecular weight: […]
cat. no. E0515
100 mM Sodium salt Solution
cat. no. E0207
100mM IPTG (Isopropyl D-thiogalacto-pyranoside) is a non-toxic, stable, filtered and ready-to-use aqueous solution. Description: IPTG is a highly stable synthetic analog of lactose. It inactivates the lac repressor and induces synthesis of beta-galactosidase. The IPTG is used to induce the expression of cloned genes which are under control of the lac operon. It is used […]
cat. no. E0601
Ultrapure set of NTPs contains four separate solutions of ATP, CTP, GTP and UTP supplied as aqueous solutions (pH 8.0). Suitable for in vitro transcription experiments. ATP Adenosine 5’-triphosphate, sodium salt. Molecular formula: C10H13N5O13P3 (Anion). Molecular weight: 504.16 (Anion) Є at absorbance max (259 nm, pH 7): 15.1 mmol-1 cm-1 CTP Cytidine 5’-triphosphate, sodium salt. […]
cat. no. E0502
Ultrapure set of dNTPs contains four separate solutions of dATP, dCTP, dGTP and dTTP supplied as aqueous solutions. dATP 2’-Deoxyadenosine 5’-triphosphate, sodium salt Molecular formula: C10H13N5O12P3 (Anion) Molecular weight: 488.16 (Anion) dCTP 2’-Deoxycytidine 5’-triphosphate, sodium salt Molecular formula: C9H13N3O13P3 (Anion) Molecular weight: 464.13 (Anion) dGTP 2’-Deoxyguanosine 5’-triphosphate, sodium salt Molecular formula: C10H13N5O13P3 (Anion) Molecular weight: […]
cat. no. E0259
RNA Loading Buffer is used as a tracking dye during RNA electrophoresis. The RNA loading dye has a slight negative charge and will migrate the same direction as RNA, allowing the user to monitor the progress of molecules moving through the gel. The rate of migration varies with gel composition. RNA Loading Buffer contains the denaturing agent […]
cat. no. E0258
RNA Loading Buffer PLUS is used as a tracking dye during RNA electrophoresis. It also contains intercalating dye Ethidium bromide for post-electrophoresis visualisation. The RNA loading dye has a slight negative charge and will migrate the same direction as RNA, allowing the user to monitor the progress of molecules moving through the gel. The rate of migration […]
cat. no. E0268
4 x Protein Loading Buffer is added to solubilized protein samples prior to analysis by SDS-polyacrylamide gel electrophoresis (SDS-PAGE). SDS detergent denatures the proteins and gives each an overall negative charge enabling proteins to migrate accordingly to their length. Glycerol increases the density of the sample so that it layers in the sample well. Bromophenol […]
cat. no. E0269
4 x Protein Loading Buffer is added to solubilized protein samples prior to analysis by SDS-polyacrylamide gel electrophoresis (SDS-PAGE). SDS detergent denatures the proteins and gives each an overall negative charge enabling proteins to migrate accordingly to their length. 2-Mercaptoethanol reduces the disulphide bonds. Glycerol increases the density of the sample so that it layers […]
cat. no. E0505
Mix of dNTPs contains dATP, dCTP, dGTP and dTTP in concentration of 5 mM each.
cat. no. E0230
5 x TBE Buffer is a sterile-filtered solution of 445 mM Tris, 445 mM boric acid and 10 mM EDTA. TBE Buffer is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis.
cat. no. E0254
Tris-glycine buffer (TG) is the common running buffer in native and gradient polyacrylamide gel electrophoresis of proteins. Tris-glycine gels resolve proteins by size. However, very small proteins and peptides do not resolve well due to interference from the glycine/pH discontinuity front. TG buffer is also used to make Tris-glycine/20% methanol Western transfer buffer, which is […]
cat. no. E0255
Tris-glycine-SDS buffer (TGS) contains the denaturing agent sodium dodecyl sulphate (SDS). Protein electrophoresis under denaturing conditions (SDS-PAGE) involves separating proteins based on their size. By treating the sample under denaturing and reducing conditions with SDS, proteins unfold and become coated with SDS detergent molecules.
cat. no. E0220
50 x TAE Buffer is a sterile-filtered solution of 2 M Tris-acetate and 50 mM EDTA. TAE Buffer is the most commonly used buffer for agarose DNA electrophoresis.
cat. no. E0260
6 x Loading Buffer BLUE is used to load DNA samples on agarose or polyacrylamide gels and to track DNA migration during electrophoresis. The buffer contains glycerol, EDTA, Xylene Cyanol and Bromophenol Blue. The glycerol increases density of sample to facilitate gel loading. EDTA inhibits metal dependent nucleases.
cat. no. E0262
6 x Loading Buffer GREEN is used to load DNA samples on agarose or polyacrylamide gels and to track DNA migration during electrophoresis. The buffer contains glycerol, EDTA, Xylene Cyanol and EURx YELLOW. The glycerol increases density of sample to facilitate gel loading. EDTA inhibits metal dependent nucleases.
cat. no. E0264
6 x Loading Buffer ORANGE is designated for preparation DNA samples for loading on agarose and polyacrylamide gels. The glycerol content increases the density of the sample and ensures that DNA form a layer at the bottom of the well. EDTA is known for inhibition of metal dependent nucleases. Tracking dyes permit monitoring of progress of electrophoresis. 1% […]
cat. no. E0261
6 x Loading Buffer RED is used to load DNA samples on agarose or polyacrylamide gels and to track DNA migration during electrophoresis. The buffer contains glycerol, EDTA, EURx RED and YELLOW. The glycerol increases density of sample to facilitate gel loading. EDTA inhibits metal dependent nucleases.
cat. no. E0265
For loading a DNA sample on agarose and polyacrylamide gels.
cat. no. E0263
6 x DNA Loading Buffer YELLOW is used to load DNA samples on agarose or polyacrylamide gels and to track DNA migration during electrophoresis. The buffer contains glycerol, EDTA and EURx Yellow. The glycerol increases density of sample to facilitate gel loading. EDTA inhibits metal dependent nucleases.
cat. no. E2004
Source: Acinetobacter calcoaceticus 5’-G T M K A C-3’ 3’-C A K M T G-5’ Reaction Temperature: 37°C Prototype: AccI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr. Total reaction volume is […]
cat. no. E2005
Source: Aeromonas caviae 5′-C A C G T G- 3′ 3′-G T G C A C- 5′ Reaction Temperature: 37°C Prototype: PmaCI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of Ad-2 DNA in 1 hr. Total reaction volume […]
cat. no. E0328
Antifoaming reagent for EURx lysis buffers. AFR01 can be used in DNA or RNA isolation procedures to reduce the foam volume generated at the lysis stage. In many cases, the first step in DNA or RNA isolation protocol is a disruption and homogenization of the sample. It is carried out in a specially composed lysis […]
cat. no. E4800
Agarase from Streptomyces sp., β-agarase cleaves β 1-4 bonds in agarose, yielding soluble oligosaccharide multimers of neoagarobiose, thus allowing for a simple, quantitative recovery of intact nucleic acids from agarose gels. Description: Digests the polysaccharide backbone of agarose yielding ethanol soluble oligosaccharides. The resulting carbohydrate molecules no longer gel or interfere with subsequent DNA manipulations. Allows […]
cat. no. E0301
Ideal for everyday analysis of nucleic acids by gel electrophoresis or blotting (Northern or Southern) and suitable for protein applications such as Ouchterlony assay and radial immunodiffusion (RID), protein electrophoresis (immunoelectrophoresis and counterelectrophoresis). Features: Low EEO. High gel strength, forming easy–to-handle gels. No DNA binding. No DNase and RNase activity. Clear and sharp bands. High […]
cat. no. E0306
Highly pure agarose recommended for DNA preparation gels. GQT (Genetic Quality Tested) certificate ensures that DNA fragments from agarose can be directly used in further procedures (restriction enzyme digestion, ligation, sequencing etc.), without the need of additional purification. Characteristics: GQT certificate Low EEO High gel strength, forming easy–to-handle gels. No DNA binding. No DNase and […]
cat. no. E0305
Agarose tablets (Molecular Biology Grade) is supplied in convenient tablet form, featuring 10 tablets in one blister pack. Agarose tablets might be used as safe and clean equivalent of agarose powder in all applications. Each agarose tablet consists 0.5 g agarose, molecular biology grade, ready to be dissolved in the appropriate amount buffer of choice. […]
cat. no. E3540
GeneMATRIX Agarose-Out DNA Purification Kit is designed to isolate ultrapure linear or circular DNA molecules, ranging in size from approximately 100 bp to 10 kb, from TAE- or TBE-agarose gels. It is also possible to purify DNA fragments up to 20 kb or more, with gradually decreasing yields. Coloured solubilizing buffer helps both in monitoring […]
cat. no. E3535
GeneMATRIX Agrobacterium Plasmid Miniprep DNA Purification Kit is designed to isolate high purity plasmid DNA from soil bacteria Agrobacterium tumefaciens. Plasmid DNA contaminants such as: RNA, singlestranded DNA, enzymes/proteins, lipids, dyes, detergents, nucleotides, EDTA, problematic restriction and ligation inhibitors, buffers and salts are effectively removed from crude bacterial lysate. The procedure is especially optimized toward […]
cat. no. E1025
Alkaline Phosphatase is calf intestine derived phosphatase which catalyzes the hydrolysis of phosphate monoesters. Has higher turnover rate and milder conditions of inactivation than bacterial enzyme. Can be used to remove 5′-phosphates from DNA or RNA prior to 5′-end labeling. Used to remove 5′-phosphates from linearized vector molecules to prevent self-ligation of the vector during […]
cat. no. E2010
Source: Arthrobacter luteus 5’- A G C T- 3’ 3’- T C G A- 5’ Reaction Temperature: 37°C Prototype: AluI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume […]
cat. no. EK2900
Amplus DNA Polymerase is a modified and optimized thermostable enzymes blend containing Thermus sp. DNA polymerase, Pyrococcus sp. DNA polymerase and the polymerase-enhancing factor. A unique composition of the amplification buffer enables effective buffering of pH at high temperatures and allows to achieve robust yield from long genomic targets. The polymerase amplifies efficiently large genomic DNA fragments from […]
cat. no. E1372
AMV Reverse Transcriptase Native, RNA dependent DNA polymerase that synthesizes a complementary DNA strand from a single-stranded RNA or DNA template in the presence of a primer. Maintains RNase H activity necessary for cDNA synthesis and isothermal RNA amplification. Can be used for preparing labeled hybridization probes. Ideal for use in RT-PCR, RAMP™, NASBA™, cDNA […]
cat. no. E0456
Description Anaplasma/Ehrlichia qPCR Detection Kit is a ready-to-use system for thedetection of Anaplasma/Ehrlichia spp. DNA in animal tissue samples (tick, mammal). The kit contains reagents and primers for the amplification ofa region of the Anaplsma/Ehrlichia genome. The detection of the Anaplasma/Ehrlichia amplicon is based on using the specific FAM-labelled probe. In addition, the kit contains a […]
cat. no. E0106
The primer mixture of a string of 20 thymidyne residues followed by dV at 3\’ end.
cat. no. E3790
AnEx Plasmid Midiprep DNA Purification Kit is designed to isolate ultrapure plasmid DNA from various species of bacteria, including recombinant Escherichia coli strains. Obtained plasmid DNA is suitable for use in routine molecular biology applications such as PCR, sequencing, transfection, in vitro transcription and translation, and enzymatic modifications. Plasmid DNA contaminants such as: RNA, single-stranded […]
cat. no. E2015
Source: Acetobacter pasteurianus 5’-G G G C C C-3’ 3’-C C C G G G-5’ Reaction Temperature: 25°C Prototype: ApaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg pXba DNA in 1 hr in a total reaction volume […]
cat. no. E0906
T3 transcription kit for synthesis of nuclease-resistant RNA. Contains a mix of NTPs with 2′–fluoro CTP and 2′-fluoro UTP. The T3 RNA Polymerase is optimized towards incorporation of 2′–fluoro modified nucleotides. Description: Incorporation of 2′-fluoro-pyrimidines protects oligonucleotides from digestion by extracellular nucleases and prolongs oligonucleotide half-life in the nuclease-rich environment (1, 3). The efficiency of […]
cat. no. E0905
T7 transcription kit for synthesis of nuclease-resistant RNA. Contains a mix of NTPs with 2’‑fluoro CTP and 2′-fluoro UTP. The T7 RNA polymerase is optimized towards incorporation of 2’‑fluoro modified nucleotides. Incorporation of 2′-fluoro-pyrimidines protects oligonucleotides from digestion by extracellular nucleases and prolongs oligonucleotide half-life in the nuclease-rich environment. The efficiency of T7 assays strongly […]
cat. no. E0457
Certified for veterinary use. Description ASFV qPCR Detection Kit is a ready-to-use system for the detection of DNA from African Swine Fever Virus in serum, plasma, blood, tissue and swab samples from pig and wild boar. The kit contains reagents and primers for the amplification of a highly conserved ASFV p72 gene fragment. The detection […]
cat. no. E2006
Source: Anabaena variabilis 5’-C Py C G Pu G -3’ 3’-G Pu G C Py C -5’ Reaction Temperature: 37°C Prototype: AvaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a […]
cat. no. E2007
Source: Anabaena variabilis 5′-G G W C C-3′ 3’-C C W G G-5’ Reaction Temperature: 37°C Prototype: AvaII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of […]
cat. no. E0446
Certified for veterinary use For influenzavirus A detection in avian samples, fast PCR
cat. no. E0445
Certified for veterinary use For influenzavirus A detection in avian samples, standard PCR
cat. no. E2003
Reaction Temperature: 37°C Inactivation Temperature: no Prototype: AvrII Isoschizomer: BlnI, XmaJI, AspA2I Source: Recombinant, purified from E.coli strain that carries the AvrII gene from Anabaena variabilis UW. Package Contents: AvrII 10x ONE Buffer BSA [100x] Added as separate component to prevent reaction buffer precipitation. Storage Conditions: Store at -20°C Double Digestion – Buffer Compatibility: ONE Buffer is compatible with […]
cat. no. E3580
GeneMATRIX Bacterial & Yeast Genomic DNA Purification Kit is designed for rapid purification of genomic DNA from a wide variety of bacterial physiological groups and from a wide variety of yeast strains. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among […]
cat. no. E2008
Source: Brevibacterium albidum 5’-T G G C C A-3’ 3’-A C C G G T-5’ Reaction Temperature: 37°C Prototype: BalI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr. Total reaction volume is 30 […]
cat. no. E2050
Source: Bacillus amyloliquefaciens H 5′-G G A T C C-3′ 3’-C C T A G G-5’ Reaction Temperature: 37°C Prototype: BamHI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total […]
cat. no. E0356
Convinient tool in spin-column format for easy and fast DNA bands extraction from TAE-agarose gels. Non DNA binding, suitable for linear and circular DNA molecules, ranging in size from approximately 70 bp to 12 kb. Prepared DNA does not require purification for further processing, including cloning or DNA sequencing. Sample volume up to 600 mg. […]
cat. no. E2060
Source: Bacillus aneurinolyticus 5’-G Pu G C Py C-3’ 3’-C Py C G Pu G-5’ Reaction Temperature: 37°C Prototype: HgiJII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E0294
Basic Cell Lysis contains phosphate inhibitors and is designed to lyse protein from adherent and suspension cultured mammalian cells and tissues, depending on nonionic detergent and recommended for cytoplasmic and membrane–bound proteins extraction. The buffer is complemented by NaF and Na3VO4 and can be used to study the phosphorylated proteins.
cat. no. E3545
GeneMATRIX Basic DNA Purification Kit is a useful basic tool in any laboratory working with DNA. It allows to perform three basic laboratory techniques: DNA purification after enzymatic treatment, isolation of DNA from agarose gels and the isolation of plasmid DNA from bacterial cultures. Combining these capabilities kit allows to streamlin work and minimizing the […]
cat. no. E0358
BeadTubeDry are used to homogenize small portions of soft animal tissues, bacterial or yeast pellets, cell cultures or environmental samples in quantities corresponding to one isolation. Each Eppendorf tube contains two types of glass spheres with 0.5 mm and 1.0 mm diameters. This selection of abrasive material allows to obtain an efficient lysis of gram-positive, gram-negative […]
cat. no. E2080
Source: Bacillus globigii RUB 561 5′-G C C N N N N N G G C-3′ 3’-C G G N N N N N C C G-5’ Reaction Temperature: 37°C Prototype: BglI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest […]
cat. no. E2090
Source: Bacillus globigii 5′-A G A T C T-3′ 3’-T C T A G A-5’ Reaction Temperature: 37°C Prototype: BglII Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E3510
GeneMATRIX Bio-Trace DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial) from the traces of biological samples (especially forensic case work samples), examplified by: fresh or frozen blood, blood spot, saliva, semen spots, hair roots and stems, cigarette filters, chewing gum, fragments of tissues, urine.The kit is effective in DNA purification […]
cat. no. E0403
Blank qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real- time RT-PCR and can be used on most real-time PCR cyclers available. The master mix does not contain any dye and allows the user to choose a dye and optimize the dye concentration. The master mix contains Perpetual Taq […]
cat. no. E0404
Blank qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real- time RT-PCR and can be used on most real-time PCR cyclers available. The master mix does not contain any dye and allows the user to choose a dye and optimize the dye concentration. The master mix contains Perpetual Taq […]
cat. no. E1410
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. This technique uses Bst polymerase which has strand displacement […]
cat. no. E1415
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. The LAMP RT technique uses reverse transcriptase, which transcribes […]
cat. no. E1411
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. This technique uses Opti Bst polymerase which has strand […]
cat. no. E1416
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. The LAMP RT technique uses reverse transcriptase, which transcribes […]
cat. no. E0298
BlueStain Sensitive is a ready-to-use stain, designed for fast and safe proteins staining. The reagent is free of methanol and acetic acid. It does not release hazardous fumes during handling and heating. Protein bands appear turquoise in color. BlueStain Sensitive detects as little as 35 ng of protein within a few minutes. Proteins stained using […]
cat. no. E0297
BlueStain Sensitive Plus is a ready-to-use stain, designed for fast and safe proteins staining. The reagent is free of methanol and acetic acid. It does not release hazardous fumes during handling and heating. Protein bands appear turquoise in color. BlueStain Sensitive Plus detects as little as 20 ng of protein within a few minutes. Proteins […]
cat. no. E3560
GeneMATRIX Bone DNA Purification Kit is designed for rapid purification of DNA (genomic, mitochondrial) from animal or human bones and teeth. Purified DNA is free of contaminants, such as: proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. A bone sample is finely grinded and the obtained powder is […]
cat. no. E0450
Borrelia qPCR Detection Kit is a ready-to-use system for the detection of Borrelia burgdorferi DNA in animal tissue samples (tick, mammal).The kit contains reagents and primers for the amplification of a 153 bp region of the Borrelia genome. The detection of the Borrelia amplicon is based on using the specific FAM-labelled probe. In addition, the […]
cat. no. E0451
Borrelia qPCR Detection Kit is a ready-to-use system for the detection of Borrelia burgdorferi DNA in animal tissue samples (tick, mammal). The kit contains reagents and primers for the amplification of a 153 bp region of the Borrelia genome. The detection of the Borrelia amplicon is based on using the specific FAM-labelled probe. In addition, the kit contains […]
cat. no. E4020
Bovine Serum Albumin acetylated to inactivate contaminating nucleases; used as a suplemment in biochemical reactions. Prolongs half-lifetime of enzymes during reaction. Suitable for dilution of restriction endonucleases and nucleic acid modifying enzymes. For use in reaction systems requiring nuclease-free bovine serum albumin. Can be used as a carrier protein for antibody production.
cat. no. E2109
Source: Bacillus stearothermophilus HKC 5’-C Py C G Pu G-3’ 3’-G Pu G C Py C-5’ Note 1: Purified from E.coli strain that carries the cloned bsiHKCRI gene. Reaction Temperature: 65°C Prototype: AvaI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest […]
cat. no. E2116
5′- T C A T G A-3′ 3′- A G T A C T-5′ Reaction Temperature: 37°C Inactivation Temperature (20 min): 80°C Prototype: BspHI Isoschizomers: PagI, RcaI Source: Recombinant. Purified from E. coli strain carrying the cloned BspHI gene. Package Contents: BspHI 10 x ONE Buffer BSA [100x] Added as separate component to prevent reaction […]
cat. no. E2115
Source: Bacillus stearothermophilus H3 5’-G C G C G C-3’ 3’-C G C G C G-5’ Reaction Temperature: 50°C Prototype: BsePI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total […]
cat. no. E1078
Large exonuclease free fragment of thermostable Bst DNA Polymerase with strand displacement activity. Bst DNA Polymerase is a moderately thermostable enzyme from Bacillus stearothermophilus. The enzyme replicates DNA optimally at 65°C. Catalyzes the polymerization of nucleotides into duplex DNA in the 5’→3′ direction in the presence of magnesium ions. Lacks the 5’→3′ exonuclease activity. The […]
cat. no. E2118
Source: Bacillus stearothermophilus X 5’-C C A N N N N N N T G G-3’ 3’-G G T N N N N N N A C C-5’ Reaction Temperature: 50°C Prototype: BstXI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x High Buffer: 50 mM Tris-HCl (pH 7.5 at 37°C), 10 mM MgCl2, 100 mM NaCl, […]
cat. no. E1450
Description: Ideal for strand displacement DNA synthesis. The enzyme replicates DNA optimally at 37°C. Devoided of both 3’→5’ exonuclease the 5’→3’ exonuclease activities, while retaining the polymerase activity. Ultrapure, recombinant enzyme. Suitable for second strand cDNA synthesis. Can be used in random primer labeling and single dA tailing. Can be heat inactivated at 75°C for […]
cat. no. E0309
Not applicable for AnEx Plasmid Midiprep DNA Purification Kit, DNA/RNA Extracol Kit and LyseBlood buffer.
While ordering please indicate the catalog number of the DNA/RNA Purification System.
cat. no. E3555
GeneMATRIX Cell Culture DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial) from animal or human cell culture. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Cells sample is lysed in the presence of special […]
cat. no. E4363
CEV qPCR Kit is intended to detect carp edema virus DNA in koi carp and common carp samples. The purified viral DNA is amplified using real-time PCR and detected using a FAM-labeled probe. The virus is identified based on a highly conserved p4a core protein gene fragment of the CEV genome. Additionally, the kit contains an […]
cat. no. E2110
Source: Caryophanon latum L 5’-A T C G A T-3’ 3’-T A G C T A-5’ Reaction Temperature: 37°C Prototype: ClaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA (dam-) in 1 hr in a […]
cat. no. E0350
Collecting tubes (2.0 ml) without caps, ready to use for all purification steps except elution.
cat. no. E2610
Color OptiTaq DNA Polymerase is a modified and optimized thermostable enzymes blend containing Thermus aquaticus DNA polymerase and Pyrococcus sp. DNA polymerase capable of generating PCR products up to 20 kb with high fidelity, suitable for applications requiring high temperature synthesis of DNA. The enzyme is supplemented with two inert gel tracking dyes. Ultrapure, recombinant enzymes […]
cat. no. E2915
Color OptiTaq PCR Master Mix (2x) is a ready-to-use solution containing OptiTaq DNA Polymerase, optimized reaction buffer, MgCl2, dNTPs and two gel tracking dyes. Use of Color OptiTaq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. OptiTaq DNA Polymerase is a modified and […]
cat. no. E2710
Ultrapure, recombinant Taq DNA Polymerase is reversibly complexed with anti-Taq monoclonal antibody that blocks replication activity of the enzyme at moderate temperatures. Our carefully selected anti-Taq antibodies have high thermal stability, providing protection against non-specific primer extension from room temperature to 70°C. The polymerase activity is restored during the initial denaturation step when amplification reactions […]
cat. no. E2745
Color Perpetual Taq PCR Master Mix (2x) is a ready-to-use solution containing Perpetual Taq DNA Polymerase, optimized reaction buffer, MgCl2, dNTPs and two gel tracking dyes. Use of Color Perpetual Taq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR setup. Color Perpetual Taq DNA […]
cat. no. E1110
Extremely thermostable proofreading DNA polymerase blend, formulated for efficient site-directed mutagenesis and synthesis of DNA products up to 20 kb. The enzyme is supplemented with two inert gel tracking dyes. Enhanced performance of PfuPlus! DNA Polymerase allows to use fewer PCR cycles and lower DNA template concentrations when compared to Pfu DNA Polymerase. Color PfuPlus! DNA […]
cat. no. E2510
Thermostable, recombinant thermophilic DNA polymerase, suitable for applications requiring high temperature synthesis of DNA. The enzyme is supplemented with two inert gel tracking dyes. The enzyme replicates DNA at 74°C and exhibits a half-life of 40 min at 95°C. Catalyzes the polymerization of nucleotides into duplex DNA in the 5´->3´ direction in the presence of magnesium […]
cat. no. E2525
Color Taq PCR Master Mix (2x) is a ready-to-use solution containing Taq DNA Polymerase, optimized reaction buffer, MgCl2 , dNTPs and two gel tracking dyes. Use of Color Taq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. Taq DNA Polymerase is a thermostable […]
cat. no. E0331
Columns for selected DNA Purification Systems, individually packed. While ordering please indicate the catalog number of the DNA Purification System.
cat. no. E0330
Columns for selected DNA Purification Systems. While ordering please indicate the catalog number of the DNA Purification System. Individually packed columns are also available.
cat. no. E0341
Columns set (binding and homogenization columns) for selected RNA Purification Systems, individually packed. While ordering please indicate the catalog number of the RNA Purification System.
cat. no. E0340
Columns set (binding and homogenization columns) for selected RNA Purification Systems. While ordering please indicate the catalog number of the RNA Purification System.
cat. no. E0110
Cut&Go gDNA Removal Kit is used for elimination of genomic DNA prior to reverse transcription. Thanks to unique thermolabile dsDNase, which is irreversibly inactivated at moderate temperature (5 minutes at 58ºC or 15 minutes at 55ºC ) RNA integrety and quality is preserved. Enzyme is highly specific towards dsDNA keeping RNA and ssDNA such as […]
cat. no. E2125
Source: Chlorella virusIL-3A 5’-Pu G C Py-3’ 3’-Py C G Pu-5’ Note 1: Purified from E.coli strain that carries the cloned cvijRI genefrom Chlorella virus IL-3A(Patent No. US005472872A) Reaction Temperature: 37°C Prototype: CviJI Inactivation Temperature (20 min): 50°C Reaction Buffer: 1x CviJI Buffer: 20 mM glycylglycine-KOH (pH 8.5), 10 mM magnesium acetate, 50 mM potassium […]
cat. no. E2126
Source: Chlorella virusIL-3A 5’-G C-3’ 3’-C G-5’ except 5’-Py G C Pu-3’ 3’-Pu C G Py-5’ Note: Purified from a recombinant source (Patent No. US005472872A) Reaction Temperature: 37°C Prototype: CviJI* Inactivation Temperature (20 min): 50°C Reaction Buffer: 1x CviJI* Buffer: 20 mM glycylglycine-KOH (pH 8.5), 10 mM magnesium acetate, 50 mM potassium acetate, 0.1 mM […]
cat. no. E2140
Source: Desulfovibrio desulfuricans 5’-C T N A G-3’ 3’-G A N T C-5’ Reaction Temperature: 37°C Prototype: DdeI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 µl. […]
cat. no. E0950
The Direct Blood PCR Kit allows to use whole blood stored at +4°C or -20°C as well as dried blood spots on cards such as commercially available Whatman FTA® cards. Blood can be preserved with all most often used anticoagulants: EDTA, citrate or heparin. It is possible to use whole blood in a wide range […]
cat. no. E0960
Direct Plant PCR Kit enables to perform PCR reactions directly from plant samples with no prior DNA purification. Description: The Direct Plant PCR Kit allows to use samples such as: plant leaves , plant seeds and plant material stored on commercially available cards. The samples can either be fresh or stored at -20°C. The Direct […]
cat. no. E0940
Direct Tissue PCR Kit enables to perform PCR reactions directly from tissue samples with no prior DNA purification. Description: The Direct Tissue PCR Kit allows to use samples such as: animal tisues, mouse ear and tail, zebrafish fin, Drosophila, human hair, saliva and other liquid samples. The samples can either be fresh or stored at […]
cat. no. E1065
DNA Ligase (E.coli) catalyzes the formation of a phosphodiester bond between juxtaposed 5’-phosphate and 3’-hydroxyl cohesive termini in duplex DNA. Catalyzes the formation of a phosphodiester bond between duplex DNA fragments with cohesive ends. Condensation of the 5′-phosphoryl group with an adjacent 3′-hydroxyl group is coupled with the hydrolysis of NAD+. Suitable for high-efficiency cloning […]
cat. no. E1075
Human DNA Polymerase Alpha is a replication enzyme used to test the toxicity of drugs on key human replication systems. It is the replication enzyme involved in initiation of DNA replication in eukaryotes. In a complex with primase, Pol α synthesizes chimeric RNA-DNA primers necessary for replication of both chromosomal DNA strands. Pol α has […]
cat. no. E1077
DNA polymerase involved in base excision and repair. A repair polymerase able to synthesize DNA beyond the end of gap or nick with simultaneous displacement of the non-replicated strand. Fills gaps or nicks.
cat. no. E1076
Mitochondrial enzyme used for testing the toxicity of drugs on critical human oxidative functions and testing replication of mitochondrial DNA. Human pol γ is isolated from mitochondria as a complex containing two subunits, a catalytic subunit, pol γA, of 139 kDa and an accessory subunit, pol γB, of 53 kDa. The catalytic subunit is a […]
cat. no. E1080
DNA Polymerase I is a mezophilic, DNA-dependent DNA polymerase with inherent 3’→5′ and 5’→3′ exonuclease activity. Exhibits the 5’→3′ polymerase activity. Used to prepare radioactive probes by nick translation and random priming. Useful for end-labeling of DNA molecules with 3’ and 5’ protruding tails or blunt-ended.
cat. no. E3750
Phenol-based reagent for the isolation of total RNA and DNA from cells and tissues in a set with minicolumns. The method is based on the extraction of nucleic acids aqueous solutions using organic solvents. After homogenizing the sample with DNA/RNA Extracol, chloroform (or 1-bromo-3-chloropropane) is added, and the homogenate is allowed to separate into a […]
cat. no. E1345
DNase I, nonspecific deoxyribonuclease that degrades both double-stranded and single-stranded DNA, endonucleolytically releasing 5′-phosphorylated di-, tri-, and oligonucleotide products. DNase I is used to remove template DNA following in vitro transcription, to remove contaminating DNA in total RNA preparations, to prepare DNA–free RNA prior to RT-PCR and RT-qPCR.
cat. no. E2135
Source: Diplococcus pneumoniae 5′-G A T C- 3′ 3′-C T A G- 5′ Purified from E.coli strain that carries the DpnI gene from Diplococus pneumoniae. Reaction Temperature: 37°C Prototype: DpnI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg […]
cat. no. E2145
Source: Deinococcus radiophilus 5’-T T T A A A-3’ 3’-A A A T T T-5’ Reaction Temperature: 37°C Prototype: AhaIII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E0473
Certified for veterinary use Description Duplex ASFV Fast qPCR Kit is intended for the detection of DNA from African swine fever virus (ASFV) in blood, serum, plasma, swab samples (from mouth, nose, nasopharynx), tissues and organs of pigs and wild boars. The high sensitivity of the kit allows the detection of the ASF virus in […]
cat. no. E0471
Certified for veterinary use For African Swine Fever Virus detection, one internal control, standard PCR
cat. no. E0453
Description Duplex Babesia qPCR Kit is a ready-to-use system for thedetection of protozoan parasite Babesia spp. in animal tissue samples (tick, mammal). The kit contains reagents and primers for the amplification ofa region of the Babesia genome. The detection of the Babesia amplicon is based on using the specific FAM-labelled probe. In addition, the kit contains […]
cat. no. E0452
Description Duplex Borrelia qPCR Kit is a ready-to-use system for the detection of Borrelia burgdorferi DNA in animal tissue samples (tick, mammal). The kit contains reagents and primers for the amplification of a region of the Borrelia genome. The detection of the Borrelia amplicon is based on using the specific FAM-labelled probe. In addition, the […]
cat. no. E0449
Description Duplex Mycoplasma qPCR Kit is a ready-to-use system for thequantitative detection of Mollicutes (Mycoplasma, Acholeplasma, Spiroplasma, Ureaplasma) DNA in cell cultures, animal tissue samples and other biological matrices. The kit enables the direct detection of all Mollicutes species known as contaminants of cell cultures. Duplex Mycoplasma qPCR Kit contains reagents and primers for the […]
cat. no. E0461
Description Duplex TBEV qRT-PCR Kit is a ready-to-use system for thedetection of TBEV RNA in animal tissue samples (tick, human). The kit detects all three TBEV subtypes: Western European, Siberian and Far Eastern subtype. Duplex TBEV qRT-PCR Kit contains reagents and primers for the amplification ofa region of the TBEV genome. The detection of the TBEV […]
cat. no. E0832
EasyJOE Multiplex Master Mix enables real-time amplification of single or multiple nucleic acid targets in easy to use One Step RT-qPCR Probe Master Mix format with the fast mode or standard cycling parameters of various thermocyclers. EasyJOE Multiplex Master Mix contains both reverse transcriptase and DNA polymerase to amplify DNA and RNA targets. The control […]
cat. no. E2150
Source: Escherichia coli RY 13 5’-G A A T T C-3’ 3’-C T T A A G-5’ Reaction Temperature: 37°C Prototype: EcoRI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a […]
cat. no. E2160
Source: Escherichia coli J62plg74 5’-G A T A T C-3’ 3’-C T A T A G-5’ Reaction Temperature: 37°C Prototype: EcoRV Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total […]
cat. no. E0355
Elution tubes (1.5 ml) ready for elution of DNA and RNA. Capped tubes to ensure no loss of sample.
cat. no. E4410
Endocyclase N15 (Protelomerase N15) catalyzes formation of covalent links between complementary 5′- and 3′- ends (clamps DNA strands together) and forms exonuclease-protected hairpin ends at specific double-stranded DNA recognition sites. Generates covalent clamps between two complementary DNA strands on one or on both ends. Converts PCR products to linear plasmids with capped “hairpin” ends. Converts […]
cat. no. E4703
C-terminal HIS-tagged full-length Enhanced Blue Fluorescent Protein, expressed in E. coli. Blue fluorescent protein (EBFP) is a genetic mutant of green fluorescent protein (GFP) originally derived from the jellyfish Aequorea victoria. Like the parent GFP, EBFP is a useful tool in cell and molecular biology. The protein is a 27 kDa monomer.
cat. no. E3572
GeneMATRIX Environmental DNA & RNA Isolation Kit is designed for rapid fractioning, isolation and purification of genomic DNA and total RNA starting from one single biological sample. Efficient lysis and cell disruption is warranted due to non-selective mechanical lysis supported by enzymatic treatment of the sample. This gives particulary good results when the bacteria are […]
cat. no. E1011
Exo-BAP Kit is used for one-step enzymatic purification of the PCR product prior to many applications such as sequencing and Single Nucleotide Polymorphism (SNP) analysis. It enables fast and efficient cleanup of any unconsumed dNTPs and primers remaining in PCR reaction without any loss of product.
cat. no. E1012
Exo-BAP Mix is used for enzymatic PCR cleanup prior to sequencing and Single Nucleotide Polymorphism (SNP) analysis. It allows quick and effective removing of any unconsumed dNTPs and primers remaining in the PCR product mixture. It contains two selected enzymes, thermosensitive bacterial alkaline phosphatase and Exonuclease I in specially composed storage buffer.
cat. no. E1150
Exonuclease I, catalyzes the removal of nucleotides from single-stranded DNA in the 3’→5′ direction. Does not degrade dsDNA or RNA. Active under a wide variety of buffer conditions. Exonuclease I is ideal for: removal of single-stranded primers in PCR reactions prior to DNA sequencing or SNP analysis, removal of single-stranded primers for nested PCR reactions, […]
cat. no. E1140
Exonuclease III catalyzes the removal of mononucleotides from dsDNA starting from a 3´-OH at nicks, blunt ends, recessed ends and 3´-overhangs of less than 4 bases, yielding nucleoside 5´-phosphates. The enzyme contains DNA 3′-phosphatase, hydrolyzing 3′-terminal phosphomonoesters and AP endonuclease, cleaving phosphodiester bonds at apurinic or apyrimidinic sites to produce 5′-termini that are base-free deoxyribose […]
cat. no. E1130
T5 Exonuclease is a product of T5 phage D15 gene derived from E. coli. T5 exonuclease degrades DNA in a 5’→3′ direction and also exhibits endonucleolytic activity on flap structures (branched duplex DNA containing a free single-stranded 5′-end). T5 exonuclease has been shown to have no effect on double stranded circular DNA.
cat. no. E1155
XRN-1 is highly processive 5´→3´ exoribonuclease, requiring 5´ monophosphate. Description: XRN-1 also acts on 5´ monophosphate ssDNA with greatly reduced efficiency. XRN-1 is not efficient in removing RNAs with recessed 5´P, like tRNA. It does not cleave dsDNA, ssDNA and RNA which contain di-, triphosphate, OH and capped 5´ ends.
cat. no. E0290
Lysis buffer with CTAB for plant tissues (pH 8.0).
cat. no. E0830
Fast MM Probe Multiplex OneStep RT-qPCR Kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets in gene expression analysis, using dual-labeled probes in easy to use master mix format. Master Mix (MM) contains all components for efficient RT-qPCR reaction with unique reverse transcriptase, highly processive hot start fast Taq DNA polymerase […]
cat. no. E1028
Thermosensitive Bacterial Alkaline Phosphatase catalyzes the release of 5′- and 3′-phosphate groups from DNA, RNA, and nucleotides. Removes 5´ phosphates from DNA, RNA, rNTPs and dNTPs. Removes 5′-phosphates from linearized vector molecules to prevent self-ligation of the vector during cloning procedures. The enzyme is resistant to chemical changes and active over a broad range of […]
cat. no. E0422
Fast Probe qPCR Master Mix (2x) is a universal solution for fast-cycling quantitative real-time PCR and two-step real-time RT-PCR using sequence-specific probes and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP). Perpetual Taq DNA Polymerase contains […]
cat. no. E0423
Fast Probe qPCR Master Mix (2x) is a universal solution for fast-cycling quantitative real-time PCR and two-step real-time RT-PCR using sequence-specific probes and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP). Perpetual Taq DNA Polymerase contains […]
cat. no. E0411
Fast SG qPCR Master Mix (2x) is a universal solution for fast-cycling quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye. SYBR Green I […]
cat. no. E0412
Fast SG qPCR Master Mix (2x) is a universal solution for fast-cycling quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye. SYBR Green I […]
cat. no. E0413
Fast SG/ROX qPCR Master Mix (2x) is a universal solution for fast-cycling quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye and ROX. SYBR […]
cat. no. E5050
Fetal Bovine Serum, originated from Brazil, certified for EU. FBS is sterile filtered and quality tested to ensure the highest quality. Fetal bovine serum is a fraction of plasma remaining after coagulation of blood, during which process the plasma protein fibrinogen is converted to fibrin and remains behind in the clot. Fetal bovine serum comes from the blood drawn from a bovine fetus via a closed […]
cat. no. E5052
Fetal Bovine Serum, originated from Colombia, certified for EU. FBS is sterile filtered and quality tested to ensure the highest quality. Fetal bovine serum is a fraction of plasma remaining after coagulation of blood, during which process the plasma protein fibrinogen is converted to fibrin and remains behind in the clot. Fetal bovine serum comes […]
cat. no. E5051
Fetal Bovine Serum heat inactivated (HI), originated from Brazil, certified for EU. FBS is sterile filtered and quality tested to ensure the highest quality. Fetal bovine serum is a fraction of plasma remaining after coagulation of blood, during which process the plasma protein fibrinogen is converted to fibrin and remains behind in the clot. Fetal bovine serum comes from the blood drawn from a bovine fetus via a […]
cat. no. E5053
Fetal Bovine Serum heat inactivated (HI), originated from Colombia, certified for EU. FBS is sterile filtered and quality tested to ensure the highest quality. Fetal bovine serum is a fraction of plasma remaining after coagulation of blood, during which process the plasma protein fibrinogen is converted to fibrin and remains behind in the clot. Fetal […]
cat. no. E3593
GeneMATRIX FFPE RNA Purification Kit is designed for rapid purification of total RNA enriched with small RNA molecules, shorter than 200 nucleotides from formalin-fixed, paraffin-embedded tissue sections. Firstly, all paraffin is removed from FFPE tissue sections by using one of deparaffinization method. Next, samples are incubated in an optimized lysis buffer, which contains Proteinase K, […]
cat. no. E0280
Reagent allows for rapid stabilizations and protection of cellular RNA against degradation. fixRNA allows for long term storage and efficient isolation of RNA at any time from animal and plant tissues, bacteria, cell cultures or leukocytes. Samples suspended within fix RNA solution are stable at room temperature for up to 7 days or at 4–8°C […]
cat. no. E1420
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. This technique uses Bst polymerase which has strand displacement […]
cat. no. E1425
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. The LAMP RT technique uses reverse transcriptase, which transcribes […]
cat. no. E1421
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. This technique uses Opti Bst polymerase which has strand […]
cat. no. E1426
LAMP (Loop-mediated isothermal amplification) is a technique for a quick amplification of nucleic acids. In contrast to the PCR technique, in which the reaction is carried out with a series of alternating temperature cycles, the LAMP reaction is carried out in a constant temperature of 65°C. The LAMP RT technique uses reverse transcriptase, which transcribes […]
cat. no. E2170
Source: Flavobacterium okeanokoites 5′-G G A T G (N)9–3′3’-C C T A C (N)13–5’ Reaction Temperature: 37°C Prototype: FokI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer It is not recommended to use more than 1 unit per 1 μg of DNA and incubate longer than 2 hours. Unit Definition: One unit is the […]
cat. no. E3525
GeneMATRIX Food-Extract DNA Purification Kit is designed for rapid purification of DNA from raw or processed food of plant, animal or mixed origin and can be used for the identification of DNA from Genetically Modified Organisms (GMO) in the food. Purified DNA is free of contaminants, such as: proteins, lipids, dyes, detergents, organic inhibitors of […]
cat. no. E3429
GeneMAGNET Blood DNA Purification Kit is designed for rapid manual or automatic purification of total DNA (genomic, mitochondrial) from fresh or frozen human blood treated with EDTA or sodium citrate anticoagulant using silica-covered magnetic beads. The new lysis buffer is specially designed to efficiently lyse blood cells, release DNA from nucelic and bind to magnetic […]
cat. no. E3427
GeneMAGNET Food DNA Purification Kit is designed for rapid purification of DNA from raw or processed food of plant, animal or mixed origin by manual or automatic method and can be used for the identification of DNA from Genetically Modified Organisms (GMO) in the food. Purified DNA is free of contaminants, such as: proteins, lipids, […]
cat. no. E3425
GeneMAGNET Human and Animal Tissue DNA Purification Kit is designed for rapid manual or automatic purification of total DNA (genomic, mitochondrial) from a variety of tissues and biological liquids. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Tissues and […]
cat. no. E3400
GeneMAGNET Magic Beads are silica coated superparamagnetic particles for nucleic acid purification. This product can be used in nucleic acids isolation (dsDNA/ssDNA/RNA) and PCR clean up. Suitable for manual and automatic applications. GeneMAGNET Magic Beads are characterized by high DNA/RNA binding capacity (>20 μg DNA/mg beads). Concentration: 50 mg/ml Very good А260/А280 ratio of the […]
cat. no. E3420
GeneMAGNET PCR / DNA Clean-Up Purification Kit is fast cleanup of DNA fragments from PCR and other enzymatic reactions. Fragment of sizes from approximately 100 bp to over 15 kb can be obtained in ultrapure form. Contaminants such as: ethidum bromide, primers (below 40 nt), short double-stranded DNA (below 20 bp), RNA, Taq DNA Polymerase, […]
cat. no. E3428
GeneMAGNET Plant DNA Purification Kit is designed for fast and easy purification of total DNA (genomic, mitochondrial and chloroplast) from a wide variety of plant, fungi and lichenes tissues. Purified DNA is free of contaminants, such as: proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Firstly, plant tissue […]
cat. no. E3401
GeneMAGNET RNA Purifictation Kit is designed for rapid, thorough isolation and purification of total RNA from a broad variety of sources: animal and human tissues, fungi, cell cultures, bacteria and yeast cells or blood (leukocytes), among others. Purified RNA is free of contaminants like proteins, nucleases, and other impurities. Samples are first lysed in the […]
cat. no. E3421
GeneMAGNET Soil DNA Purification Kit is magnetic beads based kit for the isolation of total DNA from environmental samples: soil, sediment, compost, manure, stool and water samples. Purified DNA is free of contaminants, such as: humic substances, proteins, lipids, dyes, detergents, buffers or salts. The sample is added to a tube containing glass beads and […]
cat. no. E3402
GeneMAGNET Viral RNA/DNA Purification Kit is designed for simultaneous isolation of viral RNA and DNA. The procedure is suitable for use with plasma, serum, other cell-free body fluids like milk, but also with human and animal tissues. Samples can be either fresh or frozen, assuming that they have not been frozen and thawed more than […]
cat. no. E1170
Single-stranded specific DNA binding protein from T4 bacteriophage. Reduces formation of secondary DNA structures. Prevents degradation of ssDNA by nucleases. Prevents inhibition of PCR by template DNA contaminants. Improves the efficiency of DNA amplification by Taq Polymerase. Replaces Hot Start method during assembling PCR reaction. Stabilizes single-stranded regions of DNA for site-specific mutagenesis. Aids completion […]
cat. no. E3585
GeneMATRIX Gram Plus & Yeast Genomic DNA Purification Kit is designed for the rapid purification of genomic DNA from a wide variety of gram positive bacterial physiological groups and from a wide variety of yeast strains. The mechanical lysis procedure used within protocol is a universal approach for efficient cell disruption, avoiding to use expensive […]
cat. no. E4702
C-terminal HIS-tagged full-length Green Fluorescent Protein, expressed in E. coli. Green fluorescent protein (GFP) is a cytoplasmic protein found in jellyfish Aequorea victoria (1). GFP acts as an energy transfer receptor and is actively involved in the transduction of blue chemiluminescence produced by the protein aequorin. Its main function is to convert this chemical energy into green […]
cat. no. E2180
Source: Haemophilus aegyptius 5’-G G C C-3’ 3’-C C G G-5’ Reaction Temperature: 37°C Prototype: HaeIII Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 µl. […]
cat. no. E2190
Source: Haemophilus haemolyticus 5’-G C G C-3’ 3’-C G C G-5’ Reaction Temperature: 37°C Prototype: HhaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 µl. […]
cat. no. E0302
High Resolution Agarose (Molecular Biology Grade) is an intermediate melting point agarose that efficiently separates small DNA and RNA fragments between 20 and 800 bp in length and yields ultra high resolution with high clarity and low background. Recommended applications: analysis of AFLP’s (Amplified Fragment Length Polymorphisms), STR’s (Short Tandem Repeats) and tetranucleotide repeats, recovery […]
cat. no. E2200
Source: Haemophilus influenzae Rc 5’-G T Py Pu A C-3’ 3’-C A Pu Py T G-5’ Reaction Temperature: 37°C Prototype: HindII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total […]
cat. no. E2220
Source: Haemophilus influenzae Rd 5’-A A G C T T-3’ 3’-T T C G A A-5’ Reaction Temperature: 37°C Prototype: HindIII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total […]
cat. no. E2240
Source: Haemophilus influenzae Rf 5’-G A N T C-3’ 3’-C T N A G-5’ Reaction Temperature: 37°C Prototype: HinfI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume […]
cat. no. E1373
Human Immunoeficiency Virus (HIV) Reverse Transcriptase is an RNA directed DNA polymerase which can synthesize a complementary DNA strand initiating from a primer using either RNA or single-stranded DNA as a template. Provides an excellent target for evaluating antiviral agents or inhibitors. Catalyzes error-prone synthesis on DNA and RNA templates – ideal for introducing random […]
cat. no. E2717
Description: HLA Taq DNA Polymerase is a specially formulated enzyme for HLA SSP typing using commercially available kits. HLA Taq DNA Polymerase is a new generation “hot start” enzyme that is blocked at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during normal cycling conditions. Use of HLA Taq DNA […]
cat. no. E2250
Source: Haemophilus parainfluenzae 5’-G T T A A C-3’ 3’-C A A T T G-5’ Reaction Temperature: 37°C Prototype: HpaI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E2260
Source: Haemophilus parainfluenzae 5′-C C G G-3′ 3′-G G C C-5′ Reaction Temperature: 37°C Prototype: HpaII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 μl. […]
cat. no. E2270
5′-A C N G T-3′ 3′-T G N C A-5′ Reaction Temperature: 37°C Inactivation Temperature (20 min): 65°C Prototype: Tsp4CI Isoschizomers: HpyCH4III, TaaI, Bst4CI Source: Recombinant. Purified from E. coli strain carrying the cloned HpySP4III from Helicobacter pylori sp. P4. Package Contents: HpySP4III 10 x ONE Buffer BSA [100x] Added as separate component to prevent […]
cat. no. E0440
Description HRM PCR Master Mix (2x) is designed for high-resolution melting analysis of DNA samples. HRM PCR Master Mix (2x) enables detection of gene mutations and SNPs (even the most challenging sequence differences, class III and IV SNP). The master mix contains onTaq DNA Polymerase, optimized reaction buffer, dNTPs (dATP, dCTP, dGTP, dTTP of ultrapure […]
cat. no. E3596
GeneMATRIX Human Blood RNA Purification Kit is designed for rapid purification of total RNA from fresh human blood. Purified RNA is free of contaminants, such as: DNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. In the first step the red blood cells are lysed and the remaining […]
cat. no. E4110
Human COT DNA decreases false positive signals in Microarrays, in situ Hybridizations, and Southern blots by acting as a blocking agent for repetitive sequences. EURx COT DNA has been optimized for a size range of 50 to 300 base pairs which represents the theoretical maximum size for repetitive sequences. 0,5 mg is sufficient for 5 […]
cat. no. E2950
Hybrid is a genetically engineered proofreading thermostable polymerase DNA . The enzyme catalyzes the polymerization of nucleotides into duplex DNA in the 5′->3′ direction in the presence of magnesium ions and and generates blunt ends.. The enzyme exhibits the 3′->5′ proofreading activity, resulting in over 10-fold higher PCR fidelity than possible with Taq DNA Polymerases. Enhanced […]
cat. no. E2750
Description: Hybrid PCR Master Mix (2x) is a ready-to-use solution containing Hybrid DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of Hybrid PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. Hybrid is a genetically engineered thermophilic DNA polymerase. Ultrapure recombinant enzyme. The […]
cat. no. E0834
IC-DNAJOE is a heterologous control DNA. It can be used as amplification control to exclude false-negative results caused by PCR inhibitors and as control for DNA extraction.
cat. no. E0833
IC-RNAJOE is a heterologous control RNA. It can be used as amplification control to exclude false-negative results caused by PCR inhibitors and as control for RNA extraction.
cat. no. E4361
Certified for veterinary use For IHNV detection in fish samples
cat. no. E0459
Certified for veterinary use. Influenzavirus A qRT-PCR Detection Kit is designed to detect influenzavirus A specific RNA sequences in both human and animal (including avian) samples. The purified viral genetic material is amplified by real-time RT-PCR and detected with influenzavirus A specific probes labeled with the FAM fluorescent dye. Virus identification is based on two […]
cat. no. E0205
IPTG (Isopropyl D-thiogalactopyranoside) . Description: IPTG is a highly stable synthetic analog of lactose. It inactivates the lac repressor and induces synthesis of beta-galactosidase. The IPTG is used to induce the expression of cloned genes which are under control of the lac operon. It is used in conjunction with X-Gal to determine the lac phenotype […]
cat. no. E4362
KHV qPCR Kit is intended to detect koi herpesvirus (cyprinid herpesvirus 3) DNA in koi carp and common carp samples. The purified viral DNA is amplified using real-time PCR and detected using a FAM-labeled probe. The virus is identified based on a highly conserved region in ORF 89 of the KHV genome. Additionally, the kit […]
cat. no. E1091
Klenow Fragment. Large fragment of E. coli DNA Polymerase l enzyme which retains both the polymerase and the proofreading 3’→5′ exonuclease activities of Polymerase l. Lacks the 5′-exonuclease activity. Used for Sanger dideoxy sequencing. Suitable for second strand cDNA synthesis. Used for 3′-end labeling and filling in 5′-protruding sticky ends.
cat. no. E1092
Large fragment of E. coli DNA Polymerase l, which lacks both the 3’→5′ exonuclease and the 5’→3′ exonuclease activities of Polymerase l. Used for Sanger dideoxy sequencing. Suitable for second strand cDNA synthesis. Used for 3′-end labeling and filling in 5′-protruding sticky ends.
cat. no. E2280
Source: Klebsiella pneumoniae OK 8 5’-G G T A C C-3’ 3’-C C A T G G-5’ Reaction Temperature: 37°C Prototype: KpnI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of pXba in 1 hr in a total reaction […]
cat. no. E1180
Lambda Exonuclease, double-stranded specific DNase produced by Escherichia coli upon lambda bacteriophage infection. Lambda exonuclease processively degrades one strand of double-stranded DNA (dsDNA) in the 5’→3′ direction. The preferred substrate is blunt-ended, 5´-phosphorylated dsDNA. Lambda exonuclease has reduced activity on non-phosphorylated DNA, single-stranded DNA and DNA having protruding 5′ single-stranded termini.
cat. no. E2281
Source: Recombinant. Purified from E. coli strain carrying the LlaDII from Lactococcus lactis subsp. cremoris. 5′-G C N G C-3′ 3’-C G N C G-5’ Reaction Temperature: 37°C Prototype: Fnu4HI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1 x ONE Buffer To be supplemented with 100 µg/ml bovine serum albumin. Unit Definition: One unit is the amount […]
cat. no. E0303
Low Melting Agarose is a low melting and gelling point agarose producing gels with great sieving properties and higher clarity when compared with standard agarose. Low Melting Agarose is recommended for resolving DNA and RNA fragments larger than 1000 bp and convenient recovery of nucleic acids after electrophoresis. Low Melting Agarose is ideal for in-gel […]
cat. no. E0291
Lyse Buffer PVP is recommended for the lysis of plant tissues rich in phenolic compounds and lignins. Lyse Buffer PVP contains polyvinylpyrrolidone (PVP), that binds to polyphenolics and polysaccharides that are commonly present in plant tissues and have a direct impact on the reduction of enzymatic reactions performance and efficiency. In the case of PCR/RT-PCR […]
cat. no. E0324
Solely for E3595 system. Additional lysing solution for plant tissues rich in polysaccharides.
cat. no. E0326
Buffer Lyse RBC 1x is used prior to isolation and purification of DNA or RNA from blood cells containing nuclei (leukocytes). The starting material is peripheral blood. During the procedure erythrocytes are lysed and removed together with other contaminant from plasma. Leukocytes are obtained by centrifugation in a bench centrifuge. For E3596 and E3598 RNA […]
cat. no. E4320
Lysozyme hydrolyzes the beta-glycosidic linkage between N-acetylmuramic acid and N-acetyl glucosamine in the peptidoglycan of bacterial cell walls and can also bind polymers of N-acetyl glucosamine. The enzyme is used for: cell wall degradation, preparation of protoplasts, bacteriolysis, sample preparation prior to isolation of nucleic acids. The enzyme concentration used for plasmid DNA isolation (E.coli) […]
cat. no. E0329
Lyticase is 1,3-β-Glucan glucohydrolase from Arthrobacter luteus for lysis of the fungal cell wall. Recommended to be used in DNA purification kits (Bacterial & Yeast Genomic DNA Purification Kit E3580) and RNA purification kits (Universal RNA Purification Kit E3598 and Universal DNA/RNA/Protein Purification Kit E3597). Lyticase is suspended in the storage buffer and is ready […]
cat. no. E0361
Magnetic stand for 1.5 ml or 2.0 ml Eppendorf-type tubes. Contains 16 magnets (2 rows x 8 pieces), each magnet 12 mm in diameter. For the separation of magnetic beads in the solution.
cat. no. E0362
Magnetic stand for 1.5 ml or 2.0 ml Eppendorf-type tubes. Contains 24 magnets (2 rows x 12 pieces), each magnet 12 mm in diameter. For the separation of magnetic beads in the solution.
cat. no. E0363
Magnetic stand for 96-well plate with well capacity 0.2 ml – 1.2 ml. Contains 24 magnets, 6 mm in diameter each piece. For the separation of magnetic beads in the solution.
cat. no. E2283
Source: Moraxella bovis 5’-G A T C-3’ 3’-C T A G-5’ Reaction Temperature: 37°C Prototype: MboI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Note: blocked by Dam methylation Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated lambda DNA in 1 hr in a […]
cat. no. E2284
Source: Moraxella bovis 5’-G A A G A (N)8-3’ 3’-C T T C T (N)7 -5’ Reaction Temperature: 37°C Prototype: MboII Inactivation Temperature (20 min): 65°C 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated lambda DNA in 1 hr in a total reaction […]
cat. no. E4705
C-terminal HIS-tagged full-length mCherry Fluorescent Protein, expressed in E. coli. The mCherry protein is engineered from a fluorescent protein originally isolated from a coral and is widely used as a tracer in transfection and transgenic experiments. The prototype for these fluorescent proteins is Green Fluorescent Protein (GFP), which is a ~27 kDa protein isolated originally […]
cat. no. E1402
MDA phi 29 Kit contains phi29 DNA Polymerase, that catalyzes a highly processive DNA synthesis (up to 70,000 base insertions per binding event) coupled to strand displacement activity(1). It possesses an inherent 3’-5’ exonuclease activity(2) acting preferentially on single-stranded DNA. The kit is designed to perform MDA (multiple displacement amplification) reactions. The Modified Random Hexamer […]
cat. no. E3600
Micellula DNA Emulsion & Purification Kit is designed for setting up DNA-targeted enzymatic reactions (emulsion PCR), followed by subsequent DNA purification. The kit separates individual template DNA molecules in distinct reaction compartments. This facilitates reactions starting from complex DNA fragment mixtures with partially similar sequence stretches such as complex gene libraries with identical linkers or […]
cat. no. E0292
Mild Cell Lysis is a gentle lysis solution reagent used for efficient total lysis of proteins from adherent and suspension cultured mammalian cells and tissues, depending on nonionic detergent and recommended for cytoplasmic and membrane–bound proteins extraction. Extracted proteins can be used for PAGE analysis, Western blotting, IP, ELISA.
cat. no. E0293
Mild Cell Lysis PLUS contains phosphate inhibitors and is designed to lyse protein from adherent and suspension cultured mammalian cells and tissues, depending on nonionic detergent and recommended for cytoplasmic and membrane–bound proteins extraction. The buffer is complemented by NaF and Na3VO4 and can be used to study the phosphorylated proteins.
cat. no. E2288
5′-A C G C G T-3′ 3′-T G C G C A-5′ Reaction Temperature: 37°C Inactivation Temperature (20 min): 65°C Prototype: MluI Source: Micrococcus luteus Package Contents: MluI RS* 10 x ONE Buffer BSA [100x] Added as separate component to prevent reaction buffer precipitation. Dilution Buffer # 1 Added for enzymes exceeding 10 U/µl in concentration. High […]
cat. no. E2289
Source: Moraxella nonliquefaciens 5’-C C T C (N)7 -3’ 3’-G G A G (N)6-5’ Reaction Temperature: 37°C Prototype: MnlI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume […]
cat. no. E0107
Modified Random Hexamer Primers are ready-to-use in strand displacement amplification of genomic DNA, plasmids, BACs, fosmids or phages. Modified Primers contain modified nucleotide bonds that are resistant to 3’→5′ exonuclease activity of proofreading DNA polymerases.
cat. no. E0424
MP qPCR Master Mix (2x) is a universal solution for quantitative, multiplex real-time PCR and two-step real-time RT-PCR using sequence-specific probes and can be used on most real-time PCR cyclers available. Depending on the real-time cycler used, up to 5 targets can be quantified simultaneously in the same well or tube. The master mix contains […]
cat. no. E0425
MP qPCR Master Mix (2x) is a universal solution for quantitative, multiplex real-time PCR and two-step real-time RT-PCR using sequence-specific probes and can be used on most real-time PCR cyclers available. Depending on the real-time cycler used, up to 5 targets can be quantified simultaneously in the same well or tube. The master mix contains […]
cat. no. E2290
Source: Moraxella species 5’-C C G G-3’ 3’-G G C C-5’ Reaction Temperature: 37°C Prototype: HpaII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 µl. […]
cat. no. E2820
Multiplex PCR Master Mix (2x) is developed for efficient multiplex PCR for various advanced applications. The use of the kit eliminates the need for time-consuming optimization, making the development of multiplex PCR assays easier and faster. Use of Multiplex PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting […]
cat. no. E0448
Description Mycoplasma PCR Kit is a ready-to-use system for the detection of Mollicutes (Mycoplasma, Acholeplasma, Spiroplasma, Ureaplasma) DNA in cell cultures, animal tissue samples and other biological matrices by conventional PCR. The kit enables the direct detection of all Mollicutes species known as contaminants of cell cultures. Mycoplasma PCR Kit contains reagents and primers for […]
cat. no. E0435
For SARS-CoV-2 specific genes detection in samples of various origin. Certified for veterinary use.
cat. no. E2291
Source: Nocardia argentinensis 5’-G G C G C C-3’ 3’-C C G C G G-5’ Reaction Temperature: 37°C Prototype: NarI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of pXba in 1 hr in a total reaction volume […]
cat. no. E2504
Native, thermostable DNA polymerase, suitable for applications requiring high temperature synthesis of DNA. Taq DNA Polymeraseis is purified from Thermus aquaticus. The enzyme replicates DNA at 74°C and exhibits a half-life of 40 min at 95°C. Catalyzes the polymerization of nucleotides into duplex DNA in the 5’→3′ direction in the presence of magnesium ions. Maintains […]
cat. no. E2292
Source: Nocardia corallina 5′-C C A T G G-3′ 3′-G G T A C C-5′ Reaction Temperature: 37°C Prototype: NcoI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E2293
Source: Neisseria denitrificans 5′-C A T A T G -3′ 3′-G T A T A C -5′ Reaction Temperature: 37°C Prototype: NdeI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a […]
cat. no. E0801
NG dART RT kit is first strand cDNA synthesis kit convenient for two step RT-PCR. Kit is based on modified reverse transcriptase with improved thermostability (up to 65°C) and processivity. Has easy to use format to save time and limit the possibility of pipeting errors. NG dART RT kit allows to amplify DNA from any […]
cat. no. E0802
NG dART RT-PCR kit is a first strand cDNA synthesis and PCR kit in very convenient two step format. Kit is based on modified reverse transcriptase with improved thermostability (up to 65°C) and processivity. Has easy to use format to save time and limit the possibility of pipeting errors. NG dART RT-PCR kit allows to […]
cat. no. E2294
Source: Neisseria mucosa heidelbergensis 5’-G C T A G C-3’ 3’-C G A T C G-5’ Recombinant. Purified from E.coli strain carrying the NheI gene from Neisseria nucosa heidelbergensis. Reaction Temperature: 37°C Prototype: NheI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely […]
cat. no. E2296
Source: Nocardia otitidis-caviarum 5’-G C G G C C G C-3’ 3’-C G C C G G C G-5’ Purified from an E.coli strain carrying the cloned and purified NotI gene from Nocardia otitidis-caviarum. Reaction Temperature: 37°C Prototype: NotI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount […]
cat. no. E2297
Source: Nocardia rubra 5’-T C G C G A-3’ 3’-A G C G C T-5’ Reaction Temperature: 37°C Prototype: NruI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated lambda DNA in 1 hr in a total […]
cat. no. E2298
Source: Neisseria sicca 5’-A T G C A T -3’ 3’-T A C G T A-5’ Reaction Temperature: 37°C Prototype: NsiI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume […]
cat. no. E0212
Ultrapure, deionized, sterile, nuclease-free water. Suitable for all molecular biology, DNA-targeted assays. Ideal for very sensitive detection reactions such as PCR and real time PCR.
cat. no. E2530
NXT Taq PCR Kit is designed for fast-cycling PCR on any thermal cycler. NXT Taq PCR Kit shortens PCR cycling time without affecting the yield and PCR performance. The annealing and extension steps require 5 s and 3 s per 100 bp respectively. PCR does not require redesigning of primers. Anti-Taq antibodies inhibit polymerase activity […]
cat. no. E2535
Description: NXT tiTaq PCR Kit is designed for fast-cycling PCR on any thermal cycler. NXT tiTaq PCR Kit shortens PCR cycling time without affecting the yield and PCR performance. The annealing and extension steps require 5 s and 3 s per 100 bp respectively. PCR does not require redesigning of primers. NXT tiTaq PCR Kit […]
cat. no. E0105
The solution of oligonucleotides composed of 20 deoxythymidylic acid residues. Hybridizes to the poly(A) tail of mRNA and can be used as a primer for first strand cDNA synthesis with reverse transcriptase. The primer is supplied in distilled water at a concentration of 50 μM (0.3 μg/μl).
cat. no. E1120
OMNI Nuclease catalyzes the removal of all forms of DNA and RNA (linear, circular, double and single stranded). Nuclease completely degrades nucleic acids to 5′-monophosphorate terminated oligonucleotides of 2 – 6 in length. Applications: viscosity reduction in bacterial, yeast and mammalian protein extracts, sample preparation for protein 2D electrophoresis, removal of nucleic acids contaminants from […]
cat. no. E0803
OneStep RT-PCR Kit is very convenient system for setting up one-tube RT-PCR reactions. It contains Master Enzyme Mix including highly processive dART reverse transcriptase, “hot start” DNA polymerase and unique RNase Inhibitor working well at elevated temperature. Master Buffer contains optimized buffer including dNTPs, stabilizers and reaction enhancements. Kit is designed to amplify DNA from […]
cat. no. E2960
Extremely thermostable DNA polymerase, enabling efficient high fidelity PCR of genomic targets up to 12 kb and episomal targets up to 20 kb; new generation “hot start” technology (2.0 u/µl).
cat. no. E2755
Description: onHybrid PCR Master Mix (2x) is a ready-to-use solution containing onHybrid DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of onHybrid PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR reaction setup. onHybrid DNA Polymerase contains a modified „hot start” enzyme that is […]
cat. no. E1113
Extremely thermostable hot start proofreading DNA polymerase blend, formulated for efficient site-directed mutagenesis and synthesis of DNA products up to 20 kb. Description: onPfuPlus! DNA Polymerase is a modified hot start enzyme that is blocked at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during the initial denaturation step when […]
cat. no. E2713
onTaq DNA Polymerase is a modified “hot start” enzyme which is blocked at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during 10 min initial denaturation step. Use of the onTaq DNA Polymerase allows for the increase of PCR specificity, sensitivity and yield in comparison to the conventional PCR assembly […]
cat. no. E2714
Ready-to-use solution containing onTaq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs.
cat. no. E1079
Large exonuclease 5’→3’ free fragment of thermophilic Bst DNA Polymerase with strand displacement activity. Description: Opti Bst DNA Polymerase is a moderately thermostable enzyme from Bacillus stearothermophilus genetically optimized for faster amplification and more flexible reaction conditions. Optimized for LAMP (Loop Mediated Isothermal Amplification) Enhanced dUTP incorporation compared to Bst DNA Polymerase. Ultrapure, recombinant protein. […]
cat. no. E2600
OptiTaq DNA Polymerase is a modified and optimized thermostable enzymes blend containing Thermus aquaticus DNA polymerase, Pyrococcus furiosus DNA polymerase and enhancing factors capable of generating over 20 kb products with high fidelity, suitable for applications requiring high temperature synthesis of DNA. Ultrapure, recombinant enzymes are used to prepare OptiTaq DNA Polymerase. The enzymes blend […]
cat. no. E2910
OptiTaq PCR Master Mix (2x) is a ready-to-use solution containing OptiTaq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of OptiTaq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. OptiTaq DNA Polymerase is a modified and optimized thermostable enzymes blend containing Thermus […]
cat. no. E3520
GeneMATRIX PCR / DNA Clean-Up Purification Kit is designed to isolate DNA fragments, which were subjected to or obtained as a result of various modifications and reactions: PCR products, restriction digests, after kinasing, dephosphorylation, end-trimming/repair, ligation, enzymatic or chemical modification, among others. Fragment of sizes from approximately 100 bp to over 15 kb can be […]
cat. no. E0211
Ultrapure, sterile, deionized, and prealiquoted water. The purification process for this product includes continuous deionization, reverse osmosis, UV-treatment, filtration, followed by steam sterilization in an autoclave. Suitable for use in: all PCRs and RT-PCRs, all conventional and qPCRs with any instrument, cDNA synthesis, sequencing.
cat. no. E3130
DNA ladder with 0.5-1 kb increments for sizing medium-to-large DNA fragments. Ideal for sizing linear double-stranded DNA fragments from 0.5 to 10.0 kb. Contains 11 bands with fragments of the following sizes: 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 4.0, 5.0, 6.0, 8.0, and 10.0 kb. Band at 1.0 kb is three times brighter for easy […]
cat. no. E3134
Perfect™ 100 bp DNA Ladder is DNA ladder with 100 bp increments for sizing small-to-medium DNA fragments. Ideal for sizing linear double-stranded DNA fragments from 100 to 2500 bp. Contains 13 bands with fragments of the following sizes: 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1500, 2000, 2500 bp. For easy reference, […]
cat. no. E3141
Perfect™ 100-1000 bp DNA Ladder is DNA ladder with 100 bp increments for sizing small-to-medium DNA fragments. Ideal for sizing linear double-stranded DNA fragments from 100 to 1000 bp. Contains 10 bands with fragments of the following sizes: 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000 bp. Band at 500 bp is three times […]
cat. no. E3131
Ideal for sizing linear double-stranded DNA fragments during agarose electrophoresis. Consists of 13 bands with fragments of the following sizes: 0.25, 0.5, 0.75, 1.0, 1.5, 2.0, 2.5, 3.0, 4.0, 5.0, 6.0, 8.0 and 10.0 Kb. For easy reference, bands at 1.0 and 3.0 Kb are three times brighter than other bands in the ladder. Perfect […]
cat. no. E3140
Perfect Plus™ 2 kb DNA ladder is ready to use DNA ladder for sizing small-to-large DNA fragments. Suitable for sizing linear double-stranded DNA during agarose gel electrophoresis. Consists of 8 bands with sizes of 50, 150, 300, 500, 750, 1000, 1500, and 2000 bp. For easy reference, the DNA fragment at 500 bp is three times brighter than the other bands in the ladder. Supplied […]
cat. no. E3145
Perfect Plus™ 50-500 bp DNA ladder is ready to use DNA ladder for sizing small DNA fragments. Ideal for sizing linear double-stranded DNA during agarose gel electrophoresis. Consists of 5 bands with sizes of 50, 100, 250, 400 and 500 bp. For easy reference, the DNA fragment at 250 bp is three times brighter than the other bands in the ladder. Supplied in ready-to-load buffers containing […]
cat. no. E3161
Perfect Plus™ Molecular Weight Quatitative DNA ladder is ready to use DNA ladder for sizing small-to-large DNA fragments. Ideal for sizing linear double-stranded DNA during agarose gel electrophoresis. Consists of 8 DNA fragments of the following sizes: 100, 250, 500, 750, 1000, 1500, 2000, and 5000 bp. All bands are approximately of equal intensity. Supplied in ready-to-load buffers containing tracking dyes. No preparation […]
cat. no. E3210
The Perfect™ Tricolor Protein Ladder is a prestained protein ladder, composed of precisely spaced recombinant bands, for sizing polypeptides ranging from 10 kDa to 245 kDa. The Perfect™ Tricolor Protein Ladder has twelve bands corresponding to protein size: 11, 17, 20, 25, 35, 48, 63, 75, 100, 135, 180 and 245 kDa. The 25 kDa […]
cat. no. E2720
Perpetual OptiTaq DNA Polymerase is a modified and balanced blend containing top qualityThermus aquaticus DNA Polymerase, Pyrococcus furiosus DNA Polymerase, anti-TaqDNA Polymerase antibodies, reversible inhibitors and enhancers. The polymerase activity is restored during the initial denaturation step when amplification reactions are heated at 92-95°C for two minutes. Formation of inactive complexes between Taq DNA Polymerase […]
cat. no. E2770
Perpetual OptiTaq PCR Master Mix (2x) is a ready-to-use solution containing Perpetual OptiTaq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of Perpetual OptiTaq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. Perpetual OptiTaq DNA Polymerase is a modified and balanced blend […]
cat. no. E2700
Ultrapure, recombinant Taq DNA Polymerase is reversibly complexed with anti-Taq monoclonal antibody that blocks replication activity of the enzyme at moderate temperatures. Our carefully selected anti-Taq antibodies have high thermal stability, providing protection against non-specific primer extension from room temperature to 70°C. The polymerase activity is restored during the initial denaturation step when amplification reactions […]
cat. no. E2740
Perpetual Taq PCR Master Mix (2x) is a ready-to-use solution containing Perpetual Taq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of Perpetual Taq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR setup. Perpetual Taq DNA Polymerase contains recombinant Taq DNA Polymerase bound […]
cat. no. E1114
Extremely thermostable proofreading, recombinant DNA polymerase, suitable for applications requiring high temperature synthesis of DNA. Unmodified enzyme replicates DNA at 74°C and exhibits over 95% activity after 1-hour incubation at 95°C. The enzyme catalyzes the polymerization of nucleotides into duplex DNA in the 5’→3′ direction in the presence of magnesium ions. The enzyme exhibits the […]
cat. no. E1118
Extremely thermostable proofreading DNA polymerase blend, formulated for efficient site-directed mutagenesis and synthesis of DNA products up to 20 kb. The enzyme catalyzes the polymerization of nucleotides into duplex DNA in the 5’→3′ direction in the presence of magnesium ions. The enzyme exhibits the 3’→5′ proofreading activity, resulting in over 10-fold higher PCR fidelity than possible […]
cat. no. E1401
phi29 DNA Polymerase catalyzes a highly processive DNA synthesis (up to 70,000 base insertions per binding event) coupled to strand displacement activity. It possesses an inherent 3’-5’ exonuclease activity acting preferentially on single-stranded DNA.
cat. no. E2299
Source: Pseudomonas inaequalis 5’-A C C G G T-3’3’-T G G C C A-5’ Reaction Temperature: 37°C Prototype: Age I Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E4215
RNase Inhibitor from human placenta is a pure recombinant enzyme expressed in E. coli. Placental Ribonuclease Inhibitor inhibits RNase by binding it in a 1:1 ratio with an association constant greater than 1014. Protein specifically inhibits ribonucleases A, B and C. It is not effective against RNase 1, RNase T1, S1 nuclease, RNase H or […]
cat. no. E3595
GeneMATRIX Plant & Fungi DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial and chloroplast) from a wide variety of plant, fungi and lichenes tissues. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Sample is […]
cat. no. E3500
GeneMATRIX Plasmid Miniprep DNA Purification Kit is designed to isolate very high purity plasmid DNA from various species of bacteria, including recombinant Escherichia coli strains. Plasmid DNA contaminants such as: RNA, single-stranded DNA, enzymes/proteins, lipids, dyes, detergents, nucleotides, EDTA, problematic restriction and ligation inhibitors, buffers and salts are effectively removed from crude bacterial lysate. The […]
cat. no. E1027
Thermosensitive Bacterial Alkaline Phosphatase catalyzes the release of 5′- and 3′-phosphate groups from DNA, RNA, and nucleotides. Removes 5´ phosphates from DNA, RNA, rNTPs and dNTPs. Removes 5′-phosphates from linearized vector molecules to prevent self-ligation of the vector during cloning procedures. The enzyme is resistant to chemical changes and active over a broad range of […]
cat. no. E1240
Poly (A) Polymerase is E. coli derived polymerase, polyadenylating 3′ termini of RNA. Adds poly (A) tails to the 3′-hydroxyl terminus of RNA. Ideal for determining molar concentration of polyadenylated RNA. Suitable for 3′-end labeling of RNA.
cat. no. E0307
Poly(A) – polyadenylic acid, Carrier RNA, lyophilized in small and convenient portions. The addition of carrier RNA enhances binding traces of nucleic acids to silica membranes (e.g. short DNA fragments, viral DNA/RNA). This is particularly important in cases where the sample contains very few target molecules. Poly(A) has been successfully used for PCR e.g. droplet […]
cat. no. E0820
Set of primers and synthetic RNA template for positive control of RT-PCR reaction.
cat. no. E0819
Probe Multiplex OneStep RT-qPCR kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets in gene expression analysis, using dual-labeled probes. Kit is composed of unique reverse transcriptase and highly processive hot start tiTaq DNA Polymerase in easy to use format.
cat. no. E0812
Universal solution for quantitative real-time RT-PCR with probes in single tube.
cat. no. E0813
Universal solution for quantitative real-time RT-PCR with probes in single tube with reference ROX dye.
cat. no. E0420
Probe qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains onTaq DNA Polymerase (hot start), optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP). Use of the “hot start” enzyme prevents extension of […]
cat. no. E0421
Probe qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains onTaq DNA Polymerase (hot start), optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP). Use of the “hot start” enzyme prevents extension of […]
cat. no. E4350
Proteinase K is a non-specific serine protease with a very high specific activity. It has been used for isolation of RNA, DNA and inactivation of other enzymatic activities. Proteinase K is active with or without the presence of SDS and EDTA. Proteinase K is a broad-spectrum serine protease for general digestion of proteins in biological […]
cat. no. E2300
Source: Providencia stuartii 5’-C T G C A G-3’ 3’-G A C G T C-5’ Reaction Temperature: 37°C Prototype: PstI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E2320
Source: Proteus vulgaris 5’-C G A T C G-3’ 3’-G C T A G C-5’ Reaction Temperature: 37°C Prototype: PvuI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of DNA pXba in 1 hr in a total reaction […]
cat. no. E2331
Source: Proteus vulgaris 5’-C A G C T G-3’ 3’-G T C G A C-5’ Purified from an E.coli strain carrying the cloned and purified PvuII gene from Proteus vulgaris. Reaction Temperature: 37°C Prototype: PvuII Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to […]
cat. no. E3565
GeneMATRIX Quick Blood DNA Purification Kit is designed for the rapid isolation of highly pure genomic DNA from fresh or frozen blood, serum, plasma or other body fluids. It is also possible to purify viral DNA from blood samples. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of […]
cat. no. E0101
Random Hexamer Primer is a mixture of single-stranded random hexonucleotides with 5′ and 3′ – hydroxyl ends. Random Hexamer Primers are used for priming single-stranded DNA or RNA by DNA polymerases or reverse transcriptases. Application: cDNA synthesis; in situ hybridization; DNA replication; radiolabeling of DNA probe.
cat. no. E1370
Rec A Protein is a bacterial recombination protein that enhances interaction and exchange of homologous DNA strands. It regulates repair mechanisms and repairs DNA. Involved in DNA renaturation and rare cleavage of genomic DNA. Binds cooperatively and stechiometrically to single-stranded DNA. In presence of ATP-γ-S, locates and pairs a single-stranded DNA sequence to its homologous […]
cat. no. E4704
C-terminal HIS-tagged full-length Red Fluorescent Protein, expressed in E. coli. dsRed, a tetrameric fluorescent protein cloned from the Discosoma genus of coral, has a longer wavelength substitute for green fluorescent protein (GFP) mutants for in vivo protein labeling. Bulk and single-molecule studies of the recombinant protein revealed that the dsRed chromophore shows high stability against photobleaching as […]
cat. no. E4210
Ribonuclease Inhibitor is suitable for use in all enzymatic reactions that require the inhibition of RNases present in the reaction mixture. More potent than competing human placental RNase inhibitors. RNase Free. Effective over broad pH range from pH 5.5 to 8.5. Active over temperature range from 37°C to 70°C. Does not interfere with SP6, T7 […]
cat. no. E0295
RIPA Buffer (Radioimmunoprecipitation Assay) is a complete lysis solution reagent used for rapid and efficient total lysis and solubilization of protein from both adherent and suspension cultured mammalian cells, effectively extracting cytoplasmic, nuclear and membrane proteins.
cat. no. E1280
Description: The bacterial RNA 5´ Pyrophosphohydrolase (RppH) removes pyrophosphate from the 5´ end of triphosphorylated RNA to leave a 5´ monophosphate RNA (1). The RppH protein was also known as NudH/YgdP/b2830/JW2798 which can split Ap5A to ADP and ATP (2). Could be used as alternative for TAP.
cat. no. E3700
Phenol-based reagent for the isolation of total RNA and DNA from cells and tissues. The method is based on the extraction of nucleic acids aqueous solutions using organic solvents. After homogenizing the sample with RNA Extracol, chloroform (or 1-bromo-3-chloropropane) is added, and the homogenate is allowed to separate into a clear upper aqueous layer, an […]
cat. no. E0308
RNA Storage buffer is 1 mM sodium citrate pH 6.4 in RNase-free water. The buffer is recommended for precipitate dissolving and long-term storage of RNA after e.g. RNA isolation using organic solvents like RNA Extracol (cat. no. E3700). RNA is stabilized in the solution by low pH (6.4) preventing from the nucleic acids hydrolysis and […]
cat. no. E1350
RNaza A is pyrimidine-specific endoribonuclease that acts on single-stranded RNA. RNaza A catalyzes cleavage of the phosphodiester bond between the 5′-ribose of a nucleotide and the phosphate group attached to the 3′-ribose of an adjacent pyrimidine nucleotide forming a 2′,3′-cyclic phosphate which may then be hydrolyzed to the corresponding 3′-nucleoside phosphate. A major application for […]
cat. no. E1330
RNase H (Ribonuclease H) is an RNA-specific endonuclease that cleaves the RNA of RNA/DNA hybrids. A minimum of four continuous base pairs of RNA/DNA hybrids is required for activity. RNase H cleaves RNA to release 5′-oligoribonucleotides. The enzyme does not degrade single-stranded nucleic acids, double-stranded DNA or double-stranded RNA.
cat. no. E1300
RNase I, nonspecific ribonuclease that hydrolyzes phosphodiester bond after all four bases. Only available RNase that cleaves the phosphodiester bond of all four bases. Degrades RNA to cyclic nucleotide monophosphates leaving a 5′-OH and 2′-, 3′-cyclic monophosphate. Prefers single-stranded RNA to double-stranded RNA. Contains no endonuclease or exonuclease activity toward DNA substrates. Ideal for ribonuclease […]
cat. no. E1340
RNase III is a divalent metal dependent nuclease that cleaves long, double-stranded RNA (dsRNA) into short dsRNA fragments (13-30 bases). Products of RNase III mimic siRNA structures produced by Dicer enzyme (5′-PO4, 3′-OH and a dinucleotide 3′ overhang). This unique feature enables to generate a population of RNAs that, after transfection into mammalian cells, can […]
cat. no. E0210
DEPC-treated, nuclease-free water is ideal for use in all RNA work. EURx diethyl pyrocarbonate (DEPC)-treated water is high-quality molecular grade water, guaranteed nuclease-free (tested for both DNase and RNase). The product is double-autoclaved to ensure the breakdown of DEPC.
cat. no. E2340
Source: Rhodopseudomonas sphaeroides 5’-G T A C-3’ 3’-C A T G-5’ Reaction Temperature: 37°C Prototype: RsaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction volume of 50 µl. […]
cat. no. E2342
Source: Rhodopseudomonas sphaeroides 5’-C G G W C C G-3’ 3’-G C C W G G C-5’ Purified from E.coli strain that carries the cloned rsrII gene from Rhodopseudomonas sphaeroides Reaction Temperature: 37°C Prototype: RsrII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required […]
cat. no. E1335
S1 Nuclease is non-specific endonuclease from Aspergillus oryzae, active primarily on single-stranded DNA and RNA. S1 Nuclease catalyzes degradation of single-stranded nucleic acids into oligonucleotides and 5’-mononucleotides. Double-stranded DNA, double-stranded RNA and DNA-RNA hybrids are resistant to degradation at moderate enzyme concentration. S1 Nuclease is capable of cleavage of double-stranded nucleic acids at nicks, mismatches and […]
cat. no. E2350
Source: Streptomyces achromogenes 5’-G A G C T C-3’ 3’-C T C G A G-5’ Reaction Temperature: 37°C Prototype: SacI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 μg of Lambda/HindIII DNA in 1 hr. Total reaction volume is 50 […]
cat. no. E2352
Source: Streptomyces achromogenes 5’-C C G C G G-3’ 3’-G G C G C C-5’ Reaction Temperature: 37°C Prototype: SacII Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of Ad-2 DNA in 1 hr in a total reaction […]
cat. no. E2371
Source: Streptomyces albus 5’-G T C G A C-3’ 3’-C A G C T G-5’ Purified from an E.coli strain carrying the cloned and purified SalI gene from Streptomyces albus. Reaction Temperature: 37°C Prototype: SalI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to […]
cat. no. E2375
Source: Recombinant. Purified from an E.coli strain carrying the cloned Sau3AI gene from Staphylococcus aureus 3A. 5′-G A T C-3′3′-C T A G–5′ Reaction Temperature: 37°C Prototype: MboI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x Sau3AI Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated […]
cat. no. E2379
Source: Streptomyces caespitosus 5’-A G T A C T-3’ 3’-T C A T G A-5’ Purified from an E.coli strain carrying the cloned and purified ScaI gene from Streptomyces caespitosus. Reaction Temperature: 37°C Prototype: ScaI Inactivation Temperature (20 min): 80°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required […]
cat. no. E2377
Source: Recobinant. An E. coli strain that carries the cloned ScrFI gene from Streptococcus cremoris F 5′-C C N G G-3′ 3′-G G N C C-5′ Reaction Temperature: 37°C Inactivation Temperature (20 min): 65°C Prototype: ScrFI Isoschizomers: MspR9I, Bme1390I, BmrFI Storage Conditions: Store at -20°C Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg […]
cat. no. E2381
Source: Recombinant. Purified from E. coli strain carrying the cloned SfiI gene from Streptomyces fimbriatus 5’-G G C C N N N N N G G C C-3’ 3’-C C G G N N N N N C C G G-5’ Reaction Temperature: 37°C Prototype: SfiI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE […]
cat. no. E0825
SG OneStep PRO RT-qPCR kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets. The kit consists of unique, proofreading thermostable reverse transcriptase and DNA Polymerase in an easy-to-use format. The kit provides: 2x PRO RT-qPCR SG Buffer that is a universal reaction buffer with dNTPs (dTTP is partially replaced with dUTP) […]
cat. no. E0826
SG OneStep PRO RT-qPCR kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets. The kit consists of unique, proofreading thermostable reverse transcriptase and DNA Polymerase in an easy-to-use format.
cat. no. E0811
SG OneStep RT-qPCR kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets. Kit is composed of unique reverse transcriptase and highly processive hot start onTaq DNA Polymerase in easy to use format. The use of ROX passive reference dye is necessary for all real-time PCR cyclers from Life Technologies and optional for […]
cat. no. E0810
SG OneStep RT-qPCR Kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets. Kit is composed of unique reverse transcriptase and highly processive hot start onTaq DNA Polymerase in easy to use format. During reverse transcription step at 50°C thermolabile uracil-N-glycosylase can be used. Do not use UNG from E.coli, which will degrade […]
cat. no. E0405
SG onTaq qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains onTaq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye.
cat. no. E0406
SG onTaq qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains onTaq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye. The use of ROX passive […]
cat. no. E0401
SG qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye. SYBR Green I enables DNA […]
cat. no. E0402
SG qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP) and SYBR Green I dye. SYBR Green I enables DNA […]
cat. no. E0407
Description SG/ROX onTaq qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available regardless of requirements in ROX reference dye. The master mix contains onTaq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP), SYBR Green […]
cat. no. E0400
SG/ROX qPCR Master Mix (2x) is a universal solution for quantitative real-time PCR and two-step real-time RT-PCR and can be used on most real-time PCR cyclers available. The master mix contains Perpetual Taq DNA Polymerase, optimized reaction buffer, dNTPs (dTTP is partially replaced with dUTP), SYBR Green I dye and ROX. SYBR Green I enables […]
cat. no. E3515
GeneMATRIX Short DNA Clean-Up Purification Kit is designed to isolate DNA fragments, which were subjected to or obtained as a result of various modifications and reactions: PCR products, restriction digests, after kinasing, dephosphorylation, end-trimming/repair, ligation, enzymatic or chemical modification, among others. This kit is especially optimized toward binding oligonucleotides and ds DNA molecules over the […]
cat. no. E4600
SimplySafe™ is a new and safe nucleic acid stain, an alternative to the traditional ethidium bromide (EtBr) stain for detecting nucleic acid in agarose gels. It emits green fluorescence when bound to DNA or RNA. SimplySafe™ is excitated by wavelengths emmited by traditional transiluminators. In addition, it has one visible excitation at 515 nm. SimplySafe™ […]
cat. no. E4200
Single-stranded specific DNA binding protein, helix destabilizing protein. Reduces formation of secondary DNA structures. Prevents degradation of ssDNA by nucleases. Prevents inhibition of PCR by template DNA contaminants. Improves the efficiency of DNA amplification by Taq Polymerase. Replaces Hot Start method during assembling PCR reaction. Stabilizes single-stranded regions of DNA for site-specific mutagenesis. Aids completion […]
cat. no. E2390
Source: Serratia marcescens 5′-C C C G G G-3′ 3′-G G G C C C-5′ Reaction Temperature: 25°C Prototype: SmaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 μg of Lambda/HindIII in 1 hr. Total reaction volume is 50 […]
cat. no. E0808
smART Combo First Strand cDNA Synthesis Kit for RT-qPCR is a complete system for efficient synthesis of first strand cDNA for two step real time quantitative RTPCR (RT-qPCR) applications. Kit consists of smART Reverse Transcriptase with increased thermostability and processivity and is able to sythetize cDNA from a wide range of starting total RNA (1 […]
cat. no. e0804
smART First Strand cDNA Synthesis Kit is a complete system for efficient synthesis of first strand cDNA. Kit is based on smART Reverse Transcriptase with reduced RNAse H activity, increased thermostability and processivity. The enzyme is purified from E.coli. smART is DNA polymerase that uses single-stranded RNA, DNA, or an RNA-DNA hybrid (using a primer) […]
cat. no. E1376
smART Reverse Transcriptase is a polymerase with reduced RNase H activity and increased thermal stability and processivity in the range of 37°C to 65°C . The use of the more thermostable reverse transcriptase, where reactions are performed at higher temperatures, can be very helpful when dealing with RNA that contains high amounts of secondary structure. smART is […]
cat. no. e0805
smART RT-PCR Kit is a complete system for efficient synthesis of first strand cDNA and PCR. Kit contains smART Reverse Transcriptase with reduced RNase H activity, increased thermostability and processivity. The second strand synthesis (PCR) is performed with OptiTaq DNA Polymerase.
cat. no. e0806
smART RT-qPCR Kit is a complete system for efficient synthesis of first strand cDNA and qPCR. Kit contains smART Reverse Transcriptase with increased thermostability and processivity. The real time qPCR is performed with easy to use SG qPCR Master Mix (2x). Description: Kit based on processive smART Reverse Transcriptase. Increased thermal stability of reverse transcription […]
cat. no. E0807
Complete two-step RT-PCR Kit based on smART reverse transcriptase and SG (2x) qPCR master mix with reference ROX dye.
cat. no. E0442
Description SNP Probe PCR Master Mix (2x) is designed for an accurate genotyping analysis of DNA samples. The master mix enables detection of gene mutations, SNPs and identification of microsatellite loci. SNP Probe PCR Master Mix (2x) is compatible with commercially available SNP genotyping assays as well as user-developed assays based on dual-labeled probes (TaqMan […]
cat. no. E3570
GeneMATRIX Soil DNA Purification Kit is designed for the rapid isolation of highly pure, humic-free microbial DNA from environmental samples: soil, sediment, compost, manure and filtered water samples, etc. Purified DNA is free of contaminants, such as: humic substances, proteins, lipids, dyes, detergents, buffers, salts, divalent cations, etc. Soil sample is added to a bead […]
cat. no. E4400
Sortase A is a bifunctional protein displaying both protein ligase/ transpeptidase and cysteine protease activities. Facilitates protein ligation under mild, physiological reaction conditions. Allows site-specific posttranslational generation of fusion proteins and of non-peptidic bioconjugates, which may not be synthesizable by standard molecular cloning techniques. Sortase A tolerates incorporation of oligoglycine residues containing C-terminal synthetic substituents. […]
cat. no. E1055
SpeedyLink Ligation Kit enables sticky-end or blunt-end ligation in only 5 minutes at room temperature (25°C). Fast ligation is based on the combination of T4 DNA Ligase and specially formulated buffer. It increases efficiency of ligation to that obtained with T4 DNA Ligase in a standard 1 hour ligation. After 5 min incubation DNA is […]
cat. no. E2398
Source: Sphaerotilus species 5’-A C T A G T-3’ 3’-T G A T C A-5’ Reaction Temperature: 37°C Prototype: SpeI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of pXba in 1 hr in a total reaction volume […]
cat. no. E2400
Source: Streptomyces phaeochromogenes 5’-G C A T G C-3’ 3’-C G T A C G-5’ Reaction Temperature: 37°C Prototype: SphI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E2402
Source: Sphaerotilus species 5’-A A T A T T-3’ 3’-T T A T A A-5’ Reaction Temperature: 37°C Prototype: SspI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of lambda DNA in 1 hr in a total reaction […]
cat. no. E0480
Description STEC qPCR Screening Kit is a ready to use system for the detection of Shiga toxin-producing Escherichia coli (STEC) infood and environmental samples after enrichment. The kit contains reagents and primers for the amplification of specific regions of E. coli DNA. STECs are identified based on the presence of the Shiga toxin genes (stx1 […]
cat. no. E3575
GeneMATRIX Stool DNA Purification Kit is designed for the rapid isolation of highly pure, total DNA from fresh or frozen stool samples. Purified DNA is free of contaminants, such as: enzymatic inhibitors, proteins, lipids, dyes, detergents, buffers, salts, divalent cations, etc. Stool sample is added to a bead beating tube containing beads and lysis solution. […]
cat. no. E2405
Source: Streptomyces tubercidicus 5’-A G G C C T-3’ 3’-T C C G G A-5’ Reaction Temperature: 37°C Prototype: StuI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated Lambda DNA in 1 hr in a total […]
cat. no. E5800
SV40 Large T Antigen is the major regulatory protein of SV40 virus, responsible for virion assembly, viral and cellular transcriptional regulation, viral DNA replication, alteration of the cell cycle. It also functions as molecular chaperone. SV40 Large T Antigen plays multifunctional roles: functions as an initiator protein to begin DNA replication at the SV40 origin, […]
cat. no. E3530
GeneMATRIX Swab-Extract DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial and bacterial) from the swabs taken from mucous membranes, semen, saliva or blood, among others. Purified DNA is free of contaminants, such as: proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Both freshly […]
cat. no. E1060
T4 DNA Ligase catalyzes the formation of a phosphodiester bond between juxtaposed 5’-phosphate and 3’-hydroxyl termini in duplex DNA or RNA. Catalyzes the joining of duplex DNA molecules at blunt ends. Covalently joins DNA fragments with complementary cohesive ends. Seals single-stranded nicks in duplex DNA, RNA or DNA/RNA hybrids. Suitable for cloning of restriction fragments […]
cat. no. E1100
T4 DNA Polymerase from bacteriophage T4 is the mezophilic polymerase, exhibiting very strong 3’→5′ exonuclease activity. The polymerase requires the presence of a single-stranded DNA template and a primer. Exonuclease, stronger than that found in DNA Polymerase I, is more active on single-stranded DNA than on double-stranded DNA. Exonuclease activity can be used to remove […]
cat. no. E1261
T4 Polynucleotide Kinase catalyzes the phosphorylation of 5′ hydroxyl termini of double- and single-straned DNA or RNA. Catalyzes the transfer of the γ-phosphate of ATP to a 5′-OH terminus in DNA or RNA. Contains 3′-phosphatase activity. T4 Polynucleotide Kinase is used for 5′-end labeling of nucleic acids prior to DNA or RNA sequencing. The enzyme […]
cat. no. E1059
T4 RNA Ligase 1 catalyzes the ligation of a 5´ phosphoryl-terminated nucleic acid donor to a 3´ hydroxyl-terminated nucleic acid acceptor through the formation of a 3´ → 5´ phosphodiester bond with hydrolysis of ATP to AMP and PPi. Substrates include single-stranded RNA and DNA as well as dinucleoside pyrophosphates.
cat. no. E1125
T7 Endonuclease I is an ultrapure recombinant enzyme, the product of T7 gene 3, purified from E. coli. It is structure-selective enzyme that recognizes and cleaves mismatched DNA, heteroduplex DNA, cruciform DNA structures, Holliday structures or junctions and more slowly, nicked dsDNA. The cleavage site is the first, second or third phosphodiester bond that is […]
cat. no. E1290
T7 RNA Polymerase from bacteriophage T7. Modified T7 RNA Polymerase with higher tolerance towards modified nucleotides. Extremely useful for radioactive and non radioactive labeling as well as for RNA synthesis for preparive scale. DNA-dependent RNA polymerase which has stringent specificity for T7 phage promoters sequence. Efficiently synthesizes in vitro transcripts from almost any DNA that is […]
cat. no. E0901
T7 transcription kit with modified T7 RNA Polymerase for higher tolerance towards modified nucleotides. Extremely useful for radioactive and nonradioactive labeling as well as for RNA synthesis in preparative scale. T7 RNA Polymerase is DNA-dependent RNA polymerase with stringent specificity for T7 phage promoters sequence. Efficiently synthesizes transcripts from almost any DNA target located downstream […]
cat. no. E1070
Thermostable Taq DNA Ligase catalyzes the formation of a phosphodiester bond between adjacent 5′-phosphoryl and 3′-hydroxyl cohesive termini in duplex DNA fragments. Catalyzes the formation of a phosphodiester bond between duplex DNA fragments with cohesive ends. Condensation of the 5′-phosphoryl group with an adjacent 3′-hydroxyl group is coupled with the hydrolysis of NAD+. Stable at […]
cat. no. E2500
Thermostable DNA polymerase, suitable for applications requiring high temperature synthesis of DNA. The enzyme replicates DNA at 74°C and exhibits a half-life of 40 min at 95°C. Catalyzes the polymerization of nucleotides into duplex DNA in the 5´→3´ direction in the presence of magnesium ions. Maintains the 5´->3´ exonuclease activity. Lacks the 3´→5´ exonuclease activity. […]
cat. no. E2520
Taq PCR Master Mix (2x) is a ready-to-use solution containing Taq DNA Polymerase, optimized reaction buffer, MgCl2 and dNTPs. Use of Taq PCR Master Mix (2x) allows to save time and reduce contamination risk due to fewer pipetting steps during PCR set-up. Taq DNA Polymeraseis a thermostable enzyme from Thermus aquaticus. The enzyme replicates DNA […]
cat. no. E4300
Thermostable single-stranded specific DNA binding protein from Thermus aquaticus, suitable for high temperature DNA manipulations. Helix destabilizing protein. Reduces formation of problematic secondary DNA structures. Prevents degradation of ssDNA by nucleases. Prevents inhibition of PCR by template DNA contaminants. Improves the efficiency of DNA amplification by Taq DNA Polymerase. Improves the specificity and selectivity of […]
cat. no. E2410
Source: Thermus aquaticus 5’-T C G A-3’ 3’-A G C T-5’ Reaction Temperature: 65°C Prototype: TaqI Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of unmethylated Lambda DNA in 1 hr in a total reaction volume of 50 […]
cat. no. E2411
Source: Thermus aquaticus 5’-G A C C G A (N)11–3’ 3’-C T G G C T (N) 9 -5’ Reaction Temperature: 65°C Prototype: TaqII Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Note 1: It is required to puryfy DNA before digestion. We recommend PCR / DNA Clean-Up Purification Kit or Agarose-Out DNA […]
cat. no. E1390
Terminal transferase (TdT) is a template independent polymerase that catalyzes the addition of deoxyribonucleotide monophosphate from triphosphate to the 3′ hydroxyl terminus of DNA. Prefered substrates are: single-stranded DNA, double-stranded DNA with 3’-hydroxyl termini and oligodeoxynucleotide primers. Used for specific labeling of 3′-termini with ribonucleotides. Labels 3′-ends of DNA fragments with an [ α-³²P] 3′-deoxynucleoside. […]
cat. no. E4310
Proteaza cysteinowa pochodząca z wirusa TEV (Tobacco Etch Virus) jest stosowana do usuwania znaczników powinowactwa z białek fuzyjnych w warunkach przyjaznych białkom docelowym. TEV jest proteazą cysteinową, która specyficznie rozpoznaje i rozszczepia liniowy epitop o ogólnej sekwencji E-X-X-Y-X-Q- (G/S)(2-5) (gdzie X oznacza dowolny aminokwas) (2-5). Rozszczepienie następuje między Q a G/S. Najczęstszą sekwencją jest ENLYFQG […]
cat. no. E1112
Thermostable, recombinant DNA polymerase from Thermus flavus, suitable for applications requiring high temperature synthesis of DNA. Efficiently synthesizes DNA at elevated temperatures. Can be used for high temperature DNA sequencing. Polymerase has broader Mg2+ ions concentration tolerance than Taq DNA polymerase. Can be used for amplification of nucleic acids in PCR and LCR reaction.
cat. no. E0907
Thermo T3 Transcription Kit with modified T3 RNA Polymerase for higher efficiency up to 50°C. Extremely useful for radioactive and nonradioactive labeling as well as for RNA synthesis in preparative scale. Description: DNA-dependent RNA polymerase with stringent specificity for T3 phage promoters sequence (1) and increased thermostability. Activity range: 37-51°C. Ultrapure recombinant enzyme. Efficiently synthesizes […]
cat. no. E0908
Thermo T7 Transcription Kit with modified T7 RNA Polymerase for higher efficiency up to 50°C. Extremely useful for radioactive and nonradioactive labeling as well as for RNA synthesis in preparative scale. Description: DNA-dependent RNA polymerase with stringent specificity for T7 phage promoters sequence (1) and increased thermostability. Activity range: 37-51°C. Ultrapure recombinant enzyme. Efficiently synthesizes […]
cat. no. E1251
Uracil-N-glycosylase is a pure recombinant enzyme expressed in E. coli. UNG is used in PCR and real-time PCR to prevent carryover contamination between reactions. The enzyme removes uracil from any dU-containing contaminating amplicons, leaving abasic sites and making DNA molecules susceptible to hydrolysis during the initial denaturation step. To enable PCR amplicons to be degraded, […]
cat. no. E1267
Thermostable pyrophosphatase from Thermus aquaticus, hydrolyzing inorganic pyrophosphate into phosphate. Maintains the forward direction of reactions generating pyrophosphate. Improves PCR amplification of problematic or long templates. Used as an enzyme label of ELISA.
cat. no. E1325
Thermostable RNaseH is an enzyme that specifically degrades only the RNA strand of an RNA:DNA hybrid, leaving the DNA strand and any unhybridized RNA intact. Unlike E. coli RNase H, Tth RNase H is highly active and stable at high temperatures.
cat. no. EK2930
tiAmplus DNA Polymerase is a new generation “hot start” enzyme blend that is blocked at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during normal cycling conditions. tiAmplus DNA Polymerase is a modified and optimized thermostable enzyme blend containing Thermus sp. DNA polymerase, Pyrococcus sp. DNA polymerase and the polymerase-enhancing factor. […]
cat. no. E3590
GeneMATRIX Tick RNA/DNA Purification Kit is designed for simultaneous isolation of viral and bacterial RNA and DNA that live in small arachnids or insects. The kit is optimized for the isolation of RNA and DNA from microorganisms (bacteria, viruses, fungi) that live in small (up to 5 mm long) arachnids or insects. A simple protocol […]
cat. no. E2725
tiOptiTaq DNA Polymeraseis a new generation “hot start” enzyme blend that is blocked at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during normal cycling conditions. tiOptiTaq DNA Polymerase is a modified and balanced blend containing top quality Thermus aquaticus DNA Polymerase and Pyrococcus sp. DNA Polymerase. The blend catalyzes […]
cat. no. E2726
Ready-to-use solution containing tiOptiTaq DNA Polymerase, optimized reaction buffer, MgCl₂ and dNTPs.
cat. no. E3551
GeneMATRIX Tissue & Bacterial DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial) from a variety of tissues, biological liquids, cultured cells and bacteria. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, salts, divalent cations, among others. Sample is proteolitycally […]
cat. no. E3550
GeneMATRIX Tissue DNA Purification Kit is designed for rapid purification of total DNA (genomic, mitochondrial) from a variety of fresh/frozen, paraffin-embedded or formalin-fixed (FFPE) tissues and also biological liquids like blood, saliva, plasma, urine and others. Purified DNA is free of contaminants, such as: RNA, proteins, lipids, dyes, detergents, organic inhibitors of enzymatic reactions, buffers, […]
cat. no. E0359
Tissue Grinding Tool (TGT) is a convenient tool for disrupting small portions of plant and animal tissues, bacterial, yeast or cell cultures pellets in quantities corresponding to one prep. TGT can also be used to disperse centrifugal pellets, precipitates, and other soft solids. The set consists of a 1.5 ml Eppendorf tube containing a small amount of […]
cat. no. E0357
The mini-homogenizer is a low-cost, hand-held mixing motor drive. With its greatly increased rotational speed lysis of soft tissue samples is complete in seconds.
cat. no. E2715
tiTaq DNA Polymerase is a new generation “hot start” enzyme that is blocked by a biological component at moderate temperatures and allows room temperature reaction setup. The polymerase activity is restored during normal cycling conditions. Use of tiTaq DNA Polymerase allows for the increase of PCR specificity, sensitivity and yield in comparison to the conventional PCR […]
cat. no. E2716
Ready-to-use solution containing tiTaq DNA Polymerase, optimized reaction buffer, MgCl₂ and dNTPs.
cat. no. E0472
Certified for veterinary use For African Swine Fever Virus detection, two internal controls, fast PCR
cat. no. E0470
Certified for veterinary use For African Swine Fever Virus detection, two internal controls, standard PCR
cat. no. E2502
Source: Thermus species DT 5’-A T G A A (N)11–3’ 3’-T A C T T (N) 9 -5’ Purified from E.coli strain that carries the cloned tspDTRI gene from Thermus sp. DT. Reaction Temperature: 70°C Prototype: TspDTI Inactivation Temperature (20 min): — Reaction Buffer: 1x TspDTI Buffer: 10 mM Tris-HCl (pH 8.5 at 25°C), 10 […]
cat. no. E2501
Source: Thermus species GW 5’-A C G G A (N)11–3’3’-T G C C T (N) 9 -5’ Purified from E.coli strain that carries the cloned tspGWRI gene from Thermus sp. GW. Reaction Temperature: 70°C Prototype: TspGWI Inactivation Temperature (20 min): — Reaction Buffer: 1x TspGWI Buffer: 10 mM Tris-HCl (pH 8.5 at 25°C), 1 mM […]
cat. no. E1115
Thermostable, recombinant DNA polymerase from Thermus thermophilus, exhibing reverse transcriptase acvity. Catalyzes polymerization of DNA in the presence of Mg2+ and catalyzes the reverse transcription of RNA to cDNA in the presence of Mn2+. Suitable for PCR, RT-PCR, reverse transcription and primer extension reactions at elevated temperature. Resistant to amplification inhibitors present in template DNA […]
cat. no. E1123
Endonuclease IV (Tth) is a thermostable apurinic-apyrimidinic (AP) class II DNA endonuclease from Thermus thermophilus. This enzyme is involved in the DNA base excision repair (BER) pathway, which catalyzes the cleavage of the DNA phosphodiester backbone at AP sites via hydrolysis, leaving a 1 nucleotide gap with 3′-hydroxyl and 5′ deoxyribose phosphate (dRP) termini. AP […]
cat. no. E1374
Thermus thermopilus Reverse Transcriptase catalyzes the reverse transcription of RNA to cDNA at elevated temperatures in the presence of Mn2+ and catalyzes polymerization of DNA in the presence of Mg2+. Suitable for high temperature synthesis of DNA. Synthesizes cDNA from RNA template. Minimizes problems with strong secondary structure of RNA. Used for efficient PCR of […]
cat. no. E2420
Source: Thermus thermophilus 111 5’-G A C N N N G T C-3’ 3’-C T G N N N C A G-5’ Reaction Temperature: 65°C Prototype: Tth111I Inactivation Temperature (20 min): — Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of pBC4 DNA in […]
cat. no. E4111
Uncut Human Placental DNA decreases false positive signals in Microarrays, in situ Hybridizations, and Southern blots by acting as a blocking agent for repetitive sequences.
cat. no. E3594
GeneMATRIX Universal Blood RNA Purification Kit is a specifically designed spin-column system for rapid isolation of total RNA from fresh or frozen human blood as well as from animal blood samples. Only a minimum of hands-on time is required at the sampling site: Blood samples are mixed with a specifically designed lysis buffer, which, upon […]
cat. no. E3597
GeneMATRIX DNA/RNA/Protein Purification Kit is designed for rapid purification of genomic DNA, total RNA and total protein simultaneously from a single biological sample from a wide variety of bacterial physiological groups, animal tissue, plant and from a wide variety of yeast strains. Samples are first disrupted, homogenized and lysed in the presence of lysis and […]
cat. no. e3765
Ready-to-use Genomic DNA Isolation reagent, mixture of detergents and salts for total DNA isolation from diverse samples. The method is based on the precipitation of nucleic acids from a cell lysate with ethanol. The sample is homogenized and lysed in a specially composed GeDI solution (which does not contain organic solvents such as phenol) and […]
cat. no. E0831
Universal MM Probe Multiplex OneStep RT-qPCR Kit is one-step RT-qPCR kit that provides accurate real-time quantification of RNA targets in gene expression analysis, using dual-labeled probes in easy to use master mix format. Master Mix (MM) contains all components for efficient RT-qPCR reaction with unique reverse transcriptase, highly processive hot start DNA polymerase and ROX […]
cat. no. E3760
Ready-to-use Genomic DNA Isolation reagent, mixture of detergents and salts for total DNA isolation from diverse samples.
cat. no. E3589
Universal RNA Clean-Up Kit removes DNA and other contaminants from RNA samples isolated from different sources (animal and plant tissues, bacteria, yeast, blood etc.). RNA can be purified by phenol-chloroform extraction, spin column or the use of magnetic beads. Nevertheless it is usually contaminated by genomic DNA which affects downstream applications like RT-qPCR or RNAseq. […]
cat. no. E3598
The GeneMATRIX Universal RNA Purification Kit is designed for rapid, thorough isolation and purification of total RNA from a broad variety of sources: animal, plant, fungi tissues, cell cultures, bacteria and yeast cells or blood (leukocytes), among others. Samples are first lysed in the presence of a denaturing buffer. Upon lysis buffer addition, cellular RNases […]
cat. no. E3599
GeneMATRIX Universal RNA/miRNA Purification Kit is designed for rapid purification of total RNA enriched with small RNA molecules, shorter than 200 nucleotides (also miRNA,15-30 nucleotides) or purification small RNA fraction only from animal tissue, plant or cell cultures. Samples are first disrupted, homogenized and lysed in the presence of lysis and denaturing buffers, which inactivates […]
cat. no. E1250
Uracil-N-glycosylase is a pure recombinant enzyme expressed in E. coli. UNG is used in PCR and real-time PCR to prevent carryover contamination between reactions. The enzyme removes uracil from any dU-containing contaminating amplicons, leaving abasic sites and making DNA molecules susceptible to hydrolysis during the initial denaturation step. To enable PCR amplicons to be degraded, […]
cat. no. E4360
Certified for veterinary use For VHSV detection in fish samples
cat. no. E3592
Kit for simultaneous purification of viral RNA / DNA from plasma, serum and cell-free body fluids.
cat. no. E4502
Vivid Violet DNA/RNA Co-Precipitate, highly visible inert co-precipitant designed for routine use in DNA or RNA precipitations. Vivid Violet is a neutral carrier which enhances the recovery of nucleic acids when added prior to ethanol precipitation. Results in a highly visible purple pellet after centrifugation of the precipitation mixture and thus eliminates loss of nucleic […]
cat. no. E2430
Source: Xanthomonas badrii 5’-T C T A G A-3’ 3’-A G A T C T-5’ Reaction Temperature: 37°C Prototype: XbaI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Note: blocked by overlapping Dam methylation. Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of Ad-2 DNA in […]
cat. no. E3652
XELEX kit for aptamer analysis. Contains diversity standards, DNA spin columns and components required for characterization and analysis of aptamer binding properties.
cat. no. E3650
Complete kit with all required core components for aptamer in vitro evolution and selection. Contains all components from both, XELEX selection and analysis units, respectively. Aptamers are single stranded DNA or RNA molecules with sequence-dependent three-dimensional structures. These structures allow distinct molecules to bind to target structures with high specificity and affinity by non-covalent molecular interactions. With […]
cat. no. E3651
XELEX kit for aptamer selection. Contains libraries, DNA spin columns and components required for in-vitro selection of aptamers and for intercycle library regeneration.
cat. no. E3660
The XELEX Kit series is a modular kit system covering the entire SELEX work-flow from random DNA library to RNA aptamer. This kit presents an optimized, straightforward standard operating procedure for the whole SELEX process. It consists of a core kit and several add-on packages which add functionality for individual adjustment of the selection process […]
cat. no. E2440
Source: Xanthomonas holcicola 5’-C T C G A G-3’ 3’-G A G C T C-5’ Reaction Temperature: 37°C Prototype: XhoI Inactivation Temperature (20 min): 65°C Reaction Buffer: 1x ONE Buffer Unit Definition: One unit is the amount of enzyme required to completely digest 1 µg of Ad-2 DNA in 1 hr in a total reaction volume […]
cat. no. E4701
C-terminal HIS-tagged full-length Yellow Fluorescent Protein, expressed in E. coli. Yellow fluorescent protein (YFP) is a genetic mutant of green fluorescent protein (GFP) originally derived from the jellyfish Aequorea victoria. Like the parent GFP, YFP is a useful tool in cell and molecular biology. The protein is a 26.4 kDa monomer.
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