Cytochrome P450 monooxygenase (CYP)

Description:

De CYP

ES-CYPs: Classis redox enzymorum cum mercaptan-heme sicut centrum activum ad translationem oxygenii catalysin.Eae terminales oxygenases ac necessitates heme ad activate oxygeni.

Cytochrome P450 monooxygenase oxidationis, epoxidationis et hydroxylationis alkyl, hydroxylationis et oxidationis ammoniaci, oxidationis sulphuris, dealkylationis (oxygeni, sulphuris, ammoniaci), siccitatis oxidativae, deaminationis et dehalogenationis.
Genera cytochromi P450 monooxygenas sunt octo (Number sicut ES-CYP-101～ES-CYP-108) enucleata per SyncoZymes.

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Product Detail

Product Tags

Circa CYP:

Genus reactionem catalytic:

Product Information:

Enzymes	Ornamentum protegendo (SynKit)	Specification
Enzyme Pulvis	ES-CYP-101~ ES-CYP-108	Statuto cytochrome P450 Monooxygenases, 50 mg singulorum 8 item * 50mg / item, vel alia quantitas.
Ornamentum protegendo (SynKit)	ES-CYP-800	cytochrome P450 Monooxygenases, 1mg singulae 8 items * 1mg / item

commoda:

spectro latae subiectae.
Maximum conversionem.
★ Minus per-producta.
★ Mitis reactionis condiciones.
★ Environmentally amica.

Instructiones ad usum:

➢ Communiter, systema reactionis includere debet subiectum, solutionem quiddam (optimam reactionem pH enzyme), coenzyme (NAD(H) vel NADP(H)), systema regenerationis coenzyme (eg glucose et dehydrogenas glucose) et ES-CYP.coenzyme et coenzyme systematis regenerationis reparari potuit per consectetuer peroxidum in systematis reactionis partialis.
➢ Omnia genera ES-CYPs diversis conditionibus optimae reactionis respondentes singillatim investigandae sunt.
➢ Substratum vel productum cum concentratione alto actione ES-CYP inhibere possunt.Sed inhibitio massam adiectione subiecti levari potest.

Exempla applicationis:

Exemplum 1⁽¹⁾:

Exemplum 2⁽²⁾:

Exemplum 3⁽³⁾:

Exemplum 4⁽⁴⁾:

Repono:

Custodi 2 annos infra -20℃.

Operam:

Numquam attingunt extremas condiciones ut: caliditas, alta/humilis pH et altae concentrationes organicae solvendo.

Notae:

1. Zaretzki J, Matlock M, et Swamidass S JJ Chem.Inf.Exemplar, 2013, 53, 3373-383.
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., et De Voss J J. Org.Litt., 2003, 5 (18), 3341–3344.
4. Kawauchi, H., Sasaki, J., Adachi, T., e tal.Biochim.Biophys.Acta, 1994, 1219, CLXXIX.
5. Yasutake, Y., Fujii, Y.;Cheon, WK e tal.Acta Crystallogr.MMIX, LXV, CCCLXXII.