Easy access to products and protocols for research use only in the identification of 2019-nCoV based on Centers for Disease Control and Prevention (CDC) recommendations
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Enzymes accelerate, or catalyze, chemical reactions, and they are known to catalyze more than 5,000 biochemical reaction types. Most enzymes are proteins, although a few are catalytic RNA molecules. Choose specific enzymes for cleaving bonds, removing genomic DNA from RNA preparations, for producing fragments of proteins, or for use in ion exchange chromatography. Enzymes are used in the chemical industry and other industrial applications when extremely specific catalysts are required.
Description:
Terminator* 5'-Phosphate-Dependent Exonuclease, digests RNA with 5'-monophosphate ends but not RNAs with 5'-triphosphate, 5'-cap or 5'-hydroxyl groups starting from the 5' end, Includes 10X Termina
Description:
RNase I E. Coli, Remove unwanted RNA by digesting with this heat labile, non-sequence specific ribonuclease, with dilution buffer, 10X TNE buffer, and 0.1 M DTT, RNase protection assays to detect single-basepair mismatches in
Description:
OmniCleave* Endonuclease, for Removal of nucleic acids from cell lysates (viscosity) for improved handling and yield of protein preparations, Trace contamination by nucleic acids in protein preparations, host DNA fr
Description:
Exonuclease VII, Highly specific digestion of ssDNA with both 5' to 3' and 3' to 5' exonuclease activities, Remove Epicentre Product single-stranded oligonucleotide primers after PCR, Minimize the effect of primers left over fro
Description:
RNase-Free DNase I, Digest away unwanted DNA without digesting RNA, Degrade dsDNA and ssDNA without damaging important RNA in sample or reaction, Application: Treatment of RNA prior to RT-PCR, Characterization of DNA-protein inter
Description:
Hybridase* Thermostable RNase H, Optimal activity above 65C and as high as 95 deg C, Highly specific for RNA in a RNA:DNA hybrid and will not digest free RNA or DNA, Application: High-stringency hybrid selection
Description:
Rec J Exonuclease, Magnesium-dependent digestion of single-stranded DNA in a 5' to 3' direction, Heat at 65 C for 20 minutes to kill enzyme activity, Use to remove primers from completed PCR or to degrade 1-stranded linear DN
Description:
Exonuclease I E. Coli, Processively digest ssDNA in a 3' to 5' direction without harming dsDNA - short 3' overhangs in DNA are not digested, for Removal of residual ssDNA, including oligos, from reaction mixes, ssDNA fr
Description:
Baseline-ZERO* Dnase, Effectively digest large or small dsDNA and ssDNA into mononucleotides, Digest unwanted dsDNA and ssDNA molecules including small ssDNA such as random hexamers, Includes: 10X reaction buffer and a 10X
Description:
RNA 5' Polyphosphatase, Removes the Gamma and Beta phosphates from 5'-triphosphorylated and the Beta phosphates from diphosphorylated RNA, but not dephosphorylate monophosphorylated or 5'-capped RNA, Application: Analysis
Description:
T4 Polynucleotide Kinase Cloned, Phosphorylate 5' hydroxy ends of ssDNA and dsDNA, RNA, and nucleoside 3' monophosphates, Includes 10X Reaction Buffer without ATP, Preparation of labeled DNA or RNA molecular weight mar
Description:
Exonuclease III E.coli, Digest duplex DNA in a 3' to 5' direction from a nick, blunt end, or 3'-recessed end, producing stretches of ssDNA, 10X Reaction Buffer, intermediates for site-directed mutagenesis, strand-speci
Description:
Uracil N-Glycosylase (UNG), Cleave any DNA containing dUTP, HydrolyzesEpicentre Product the N-glycosidic bond between the deoxyribose sugar and uracil in DNA containing deoxyuridine in place of thymidine, for use in
Enzymes
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