Manufacturing Companies for Nmn Plus Supplement - Cytochrome P450 monooxygenase (CYP) – SyncoZymes

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Good quality To start with,and Purchaser Supreme is our guideline to offer the top service to our customers.Presently, we've been seeking our best to be amongst the top exporters inside our industry to fulfill consumers extra need to have for Pure Nadh , Nmn Pure Powder , Nmn Supplement , All prices depend upon the quantity of your respective order; the extra you purchase, the extra economical the rate is. We also offer fantastic OEM provider to numerous famous brands.

Manufacturing Companies for Nmn Plus Supplement - Cytochrome P450 monooxygenase (CYP) – SyncoZymes Detail:

Catalytic reaction type:

cyp
cyp1
cyp2
cyp3

Enzymes	Screening Kit (SynKit)	Specification
Enzyme Powder	ES-CYP-101~ ES-CYP-108	a set of 8 Cytochrome P450 Monooxygenases, 50 mg each 8 items * 50mg / item, or other quantity
Screening Kit (SynKit)	ES-CYP-800	a set of 8 Cytochrome P450 Monooxygenases,1mg each 8 items * 1mg / item

★ Broad substrate spectrum.
★ High conversion.
★ Less by-products.
★ Mild reaction conditions.
★ Environmentally friendly.

➢ Normally, the reaction system should include substrate, buffer solution (The optimum reaction pH of enzyme), coenzyme (NAD(H) or NADP(H)), coenzyme regeneration system (e.g. glucose and glucose dehydrogenase) and the ES-CYP. coenzyme and coenzyme regeneration system could be replaced by hydrogen peroxide in partial reaction system.
➢ All kinds of ES-CYPs corresponding to various optimum reaction conditions should be studied individually.
➢ High concentration Substrate or product with may inhibit ES-CYP’s activity. However, the inhibition can be relieved by batch addition of substrate.

Example 1 ⁽¹⁾:

cpyExample1

Example 2 ⁽²⁾:

cpyExample2

Example 3⁽³⁾:

cpyExample3

Example 4⁽⁴⁾:

cpyExample4

Keep 2 years below -20℃.

Never contact with extreme conditions such as: high temperature, high/low pH and high concentration organic solvent.

1. Zaretzki J, Matlock M, and Swamidass S J. J. Chem. Inf. Model, 2013, 53, 3373–3383.
2. Gannett P M., Kabulski J, Perez F A., e tal. J. Am. Chem. Soc., 2006, 128 (26), 8374–8375.
3. Cryle M J., Matovic N J., and De Voss J J. Org. Lett., 2003, 5 (18), 3341–3344.
4. Kawauchi, H., Sasaki, J., Adachi, T., e tal. Biochim. Biophys. Acta, 1994, 1219, 179.
5. Yasutake, Y., Fujii, Y.; Cheon, W. K. e tal. Acta Crystallogr. 2009, 65, 372.

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