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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:
Beta-N-Acetylglucosaminidase S, is a highly specific exoglycosidase that catalyzes the hydrolysis of terminal, non-reducing b-N-Acetylglucosamine residues from oligosaccharides. - 100 units
Description:
PNGase A, 5,000 units/ml, PNGase A is a recombinant amidase, which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and short complex oligosaccharides such as those found in plant and insect cells from N-linked glycoproteins and glycopeptides. 150 units
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: 1250 units
Description:
PNGase F (Glycerol-free), Recombinant, cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins, Source:Cloned from Elizabethkingia miricola, 75, 000 units
Description:
TelN Protelomerase, Isolated from phage N15, Cuts dsDNA at a TelN recognition sequence (56 bp), Leaves covalently closed ends at the site of cleavage, Tel N is an Enzyme for Innovation, Concentration: 5, 000 units/ml, Size: 250 units
Description:
1 kilounit CAS: 9001-40-5, MDL: MFCD00081656 Lyophilized powder Oxidizes glucose-6-phosphate in the presence of NADP+ to yield 6-phosphogluconate
Description:
Exonuclease VII, (Exo VII) derived from E. coli, cleaves single-stranded DNA (ssDNA) from both 5'→3' and 3'→5' direction, for removal of single stranded oligonucleotide primers (3) from a completed PCR reaction, 200 units
Description:
Exonuclease VII, (Exo VII) derived from E. coli, cleaves single-stranded DNA (ssDNA) from both 5'→3' and 3'→5' direction, for removal of single stranded oligonucleotide primers (3) from a completed PCR reaction, 1, 000 units
Description:
Nb.BssSI - 1,000 units Nicking Endonucleases can generate nicked or gapped duplex DNA for studies of DNA mismatch repair and for diagnostic applications. The long overhangs that nicking enzymes make can be used in DNA fragment assembly.
Description:
Proteinase K (PK) Solution, produced by the fungus Tritirachium album Limber, is a serine protease that exhibits broad cleavage activity, stability: urea and SDS, Application: pulsed-field gel electrophoresis, protein fingerprinting, Concentration: 20mg/ml, Size: 16ml
Description:
Proteinase K, 100mg, is a highly active serine protease with broad cleavage specificity on native and denatured proteins. For purification of native RNA and DNA from tissues or cell lines, as well as for many other applications.
Description:
Modifying enzyme. Labeling in vitro, sequencing, mapping, mutagenesis, duplex shortening. 150-200 units/uL. Size: 5000 units. In a tamper-evident, clear plastic sealed packet with enzyme tube, its buffer(s) and a lot-specific Promega* Product Information insert. 24-month lifetime.
Description:
Thermolabile Exonuclease I, DNA specific exonuclease, Removal of single-stranded primers in PCR, Removal of single-stranded primers for nested PCR reactions, Removal of linear single-stranded DNA, leaving behind double-stranded DNA, 20000 units/ml, 15000 units
Description:
Modifying enzyme. Labeling in vitro, ligation. Concentration: 1 unit/uL. 1000 units. Packaged in a tamper-evident, clear plastic sealed packet that contains the enzyme tube, its buffer(s) and a lot-specific Promega* Product Information insert. 24-month lifetime.
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