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:
Crystalline suspension in 3.2 M (NH4)2SO4, 10 mM MgCl2, 10 mM Tris, pH 7.5. Catalyzes the hydrolysis of N-terminal residues from di- and tripeptides. Activity: 50 units/ml. Specific activity: 10 units/mg protein.
Description:
Trichoderma viride Form Yellowish white solid Cas number 9012-54-8 Storage +2C to +8C.Hydrolyzes Beta 1,4-glucan linkages in cellulose. Has been used to isolate intact cells and protoplasts from plant tissues.1 KU = 1000 units.
Description:
Recombinant Human Enterokinase is expressed as a linear 1019 amino acid polypeptide precursor glycoprotein with molecular weight of 108.7 kDa, Animal free, Source: CHO cells, Purity: Greater than 90% by SDS-PAGE gel and HPLC analyses, 100UG
Description:
[2-(4-Imidazolyl)ethylamine]. Potent vasodilator found in normal tissues and blood. Activates nitric oxide synthase. Formed by the decarboxylation of L-histidine. Purity: >99% by TLC. Soluble in water. CAS: 51-45-6. FW: 111.2. Off-white solid, 5g.
Description:
Effective Viscosity Reduction and Removal of Nucleic Acids from protein solutions, Purity > 99% by SDS-PAGE, Total endotoxin: < 0.25 EU/1000 units, Storage -20degreeC, Nuclease is a genetically engineered endonuclease from Serratia marcescens
Description:
Ribonuclease R (RNase R), from E. Coli is a magnesium-dependent 3' to 5' exoribonuclease that digests all linear RNAs except lariat or circular RNA structures, with a 10X Reaction Buffer, Application: Alternative splicin
Description:
One unit is defined as the amount of enzyme that causes a ΔA260 of 1.0 in 30 minutes, which corresponds to complete digestion of 37 ug DNA, Purity Purity: > 90% by SDS-PAGE, Storage -20degreeC
Description:
Plasmid-Safe* ATP-Dependent Dnase, Remove contaminating bacterial chromosomal DNA from plasmid, cosmid, fosmid, and BAC preps, without digesting nicked or closed-circular dsDNA, Includes: 10X Reaction Buffer a
Description:
Lyophilized from 200 mM NaCl, 50 mM sodium citrate, 0.1% PEG, pH 6.5. Designed for use in thrombin time tests. Specific activity: 2800 NIH units/mg protein.
Description:
Trichoderma viride Form Yellowish white solid Cas number 9012-54-8 Storage +2C to +8C.Hydrolyzes Beta 1,4-glucan linkages in cellulose. Has been used to isolate intact cells and protoplasts from plant tissues.1 KU = 1000 units.
Description:
Recombinant Rat Carboxypeptidase-B is a 35.1 kDa protein consisting of 307 amino acids, Animal free, Source: E.coli, Purity: Greater than 95% by SDS-PAGE gel and HPLC analyses, Synonyms: Cpb1, 250ug
Description:
Recombinant Mycoplasma Arginine Deiminase, 46.3kda protein consist of 409AA, microbial enzyme from Mycoplasma produced in E.coli.It has high affinity to L-arginine and hydrolyzes L-arginine to citrulline and ammonia, Source: E.coli, >97%, Synonym: ADI, 20UG
Description:
Recombinant Human Enterokinase is expressed as a linear 1019 amino acid polypeptide precursor glycoprotein with molecular weight of 108.7 kDa, Animal free, Source: CHO cells, Purity: Greater than 90% by SDS-PAGE gel and HPLC analyses, 500UG
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
Description:
(b-D-Galactoside galactohydrolase). Lyophilized solid. Inducible enzyme not found in eukaryotic cells that is used as a reporter gene. Used to assess efficiency of transfection. Also used in ELISA and immunocytochemical techniques.
Description:
10ug liquid in 150mM NaCl, 50mM HEPES, pH 7.6. Purity>=95% by SDS-PAGE. Molecular weight: 700kDa. Hydrolyzes various peptide substrates and proteins with broad specificity in non-ATP-dependent process. Can be activated by PA28 or SDS.
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
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