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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:
APE 1, also known as HAP 1 or Ref-1, shares homology with Escherichia coli exonuclease III protein, with NEBuffer 4, Source: E. Coli strain, Concentration: 10X, Applications: Comet assay, Alkaline elution, Alkaline unwinding, Modified nick translation, Size: 1,000 units
Description:
10mg CAS: 9054-89-1, MDL: MFCD00132404 Lyophilized powder Catalyzes the dismutation of superoxide radicals to hydrogen peroxide and molecular oxygen
Description:
Pngase F Catalyzes The Cleavage Of N-Linked Oligosaccharides Between The Innermost Glcnac And Asparagine Residues Of High Mannose, Hybrid And Complex Oligosaccharides From N-Linked Glycoproteins.
Description:
RNase H (Ribonuclease H)endoribonuclease, Concentration: 5,000 units/ml, hydrolyzes the phosphodiester bonds of RNA which hybridized to DNA, enzyme does not digest single/double-stranded DNA, Source: E. Coli, Reagent: RNase H Reaction Buffer (10X Concentration), Size: 250 units
Description:
Proteinase K solution, ReliaPrep* Large Volume HT gDNA Isolation System, isolates genomic DNA (gDNA) from 1 to 10ml of blood in a scalable format, eliminates tedious centrifugation steps as well as the use of hazardous chemicals, size: 23ml
Description:
Arg-C (clostripain) is an endopeptidase that cleaves at the C-terminus of arginine residues, including the sites next to proline. Cleavage also will occur at lysine residues. Can be used alone or in combination with other proteases for protein analysis.
Description:
Alpha 2-3, 6, 8, 9 Neuraminidase A, catalyzes the hydrolysis of all linear and branched non-reducing terminal sialic acid residues from glycoproteins and oligosaccharides, Cloned from Arthrobacter ureafaciens and expressed in E. coli (2). - 4,000 units
Description:
For sequencing, mutagenesis, cDNA synthesis, cDNA cloning, primer extension. Concentration: 5-10units/uL. 1000 units. In a tamper evident, plastic sealed packet. Contains the enzyme tube, its buffer(s) and lot-specific Promega* Product Information. 24-month lifetime.
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