Modifying Enzymes
Abcam NADP, Coenzyme, 250MG
MW 787.37 g/mol, Purity >=93%. NADP and NADPH form a redox pair. NADP is the oxidised form of NADPH. NADP/NADPH is a coenzyme that supports redox reactions via the transport of electrons in a vast array of applications. Acts as a coenzyme couple in various cytochrome P450 systems and oxidase/reductase reaction systems.
The product is subject to the following: Abcam Restricted Use Statement
Worthington Biochemical Corporation TRYPSIN 3X TRL3 1GM
Trypsin, 3X, 1g, Crystallized, Dialyzed Against 1mM HCl and Lyophilized, 2degree to 8degreeC Storage Temp, Source: Bovine Pancreas
Sigma Aldrich Fine Chemicals Biosciences Glucose Oxidase from Aspergillus niger | 9001-37-0 | MFCD00131182 | 2.5mu
Glucose Oxidase from Aspergillus niger | 9001-37-0 | MFCD00131182 | 2.5mu
Apexbio Technology LLC Phusion high-fidelity DNA polymerase, 500U
Phusion high-fidelity DNA polymerases are composed of a DNA-binding domain fused to a Pyrococcus-like proofreading polymerase. Because of this, Phusion DNA polymerases produce PCR products with very high speed and accuracy. Also, Phusion DNA polymerases are tolerant of various inhibitors, allowing for robust amplification with minimal optimization. Phusion DNA Polymerase is an ideal choice for cloning and can be used for long or difficult (GC-rich) amplicons. Phusion high-fidelity DNA polymerases have become the choice for even demanding applications like massively parallel high-throughput sequencing of whole genomes. Other sizes are also available. Please inqury us for quote.
New England Biolabs, Inc. PNGase F – 75000 units
PNGase F is the most effective enzymatic method for removing almost all N-linked oligosaccharides from glycoproteins. PNGase F is an amidase, which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides.
- Leaves N-glycan core oligosaccharides intact and suitable for further analysis
- Non-recombinant with no detectable endoglycosidase F1, F2 or F3 contamination
- >= 95% purity, as determined by SDS-PAGE and intact ESI-MS
- Stored in 50% glycerol
- Optimal activity and stability for up to 24 months
- Can be used under native or denaturing conditions
Sigma Aldrich Fine Chemicals Biosciences Peroxidase from horseradish Type VI, essentially salt-free, lyophilized powder, ≥250 units/mg solid (using pyrogallol) | 9003-99-0 | MFCD00071339 | 10ku
Peroxidase from horseradish Type VI, essentially salt-free, lyophilized powder, ≥250 units/mg solid (using pyrogallol) | Purity: | MW: | 9003-99-0 | MFCD00071339 | 10ku
Sigma Aldrich Fine Chemicals Biosciences Catalase from bovine liver | 9001-05-2 | MFCD00081483 | 100mg
Catalase from bovine liver | Mol Wt: tetramer -250 kDa | 9001-05-2 | MFCD00081483 | 100mg
Sigma Aldrich Fine Chemicals Biosciences Lipase from Pseudomonas cepacia powder, light beige, >=30 U/mg | 9001-62-1 | MFCD00131509 | 100MG
Lipase from Pseudomonas cepacia powder, light beige, >=30 U/mg | 9001-62-1 | MFCD00131509 | 100MG
Bio IVT Human Aldehyde Oxidase; cytosolic extract of the fULl-length recombinant protein expressed in E. coli, 250UL
Human Aldehyde Oxidase; cytosolic extract of the fULl-length recombinant protein expressed in E. coli, 250UL
Sigma Aldrich Fine Chemicals Biosciences Butyryl coenzyme A lithium25MG
Butyryl coenzyme A lithium25MG
Sigma Aldrich Fine Chemicals Biosciences beta-Glucuronidase from Helix pomatia Type H-1, partially purified powder, >=300,000 units/g solid | 9001-45-0 | MFCD00130629 | 100KU
beta-Glucuronidase from Helix pomatia Type H-1, partially purified powder, >=300,000 units/g solid | 9001-45-0 | MFCD00130629 | 100KU
AG Scientific Inc Cholesterol Esterase 100 U
Cholesterol esterase catalyzes the hydrolysis of sterol esters into their component sterols and fatty acids. The enzyme is found primarily in the pancreas, but has been detected in other tissues as well. Bile salts, such as cholate and its conjugates, are required to stabilize the enzyme in its native polymeric form and to protect it from proteolytic hydrolysis in the intestine.Cholesterol esterase is used for determination of cholesterol in serum and plasma, with cholesterol oxidase or peroxidase and synthesis of optically active alcohols and carboxylic acids. Its activators are Bile salts, Cholate, Glycocholate, Taurocholate and inhibitors are PMSF and p-chloromercuribenzoate, Diisopropyl fluorophosphate, Hg2+, Ag+, and ionic detergents, Aryl carbamates.
New England Biolabs, Inc. Bpu10I – 200 units
A restriction endonuclease that recognizes the sequence CC^TNA_GC.