49854
Alcohol Dehydrogenase, recombinant from E. coli
5.0-15.0 U/mg
Synonym(s):
Alcohol:NADP+ oxidoreductase
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
CAS Number:
UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
232-823-8
MDL number:
Specific activity:
5.0-15.0 U/mg
Recombinant:
expressed in E. coli
recombinant
expressed in E. coli
form
crystals, powder or crystals
specific activity
5.0-15.0 U/mg
solubility
50 mM phosphate buffer pH 7.0: 1 mg/mL, clear to faintly turbid, slightly yellow to deep brownish-yellow
storage temp.
−20°C
Looking for similar products? Visit Product Comparison Guide
Other Notes
1 U corresponds to the amount of enzyme which reduces 1 μmol acetone per minute at pH 7.0 and 30°C (NADPH as cofactor)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
常规特殊物品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Alcohol dehydrogenase-catalyzed synthesis of enantiomerically pure d-lactones as versatile intermediates for natural product synthesis.
Fischer, T. and Pietruszka, J.
Advanced Synthesis & Catalysis, 354, 2521-2530 (2012)
Chemo-promiscuity of alcohol dehydrogenases: reduction of phenylacetaldoxime to the alcohol.
Ferreira-Silva, B., et al.
Tetrahedron, 66, 3410-3414 (2010)
Günter E Jeromin
Biotechnology letters, 31(11), 1717-1721 (2009-07-01)
A new immobilisate of alcohol dehydrogenase (ADH) is described in which all components for the reaction, i.e. enzyme, the coenzyme NADP(+), the buffer and other cofactors (trace elements), are immobilized together. It is an all-inclusive catalyst. The support is a
Alexandra Lerchner et al.
Biotechnology and bioengineering, 110(11), 2803-2814 (2013-05-21)
The NADP⁺-dependent alcohol dehydrogenase from Ralstonia sp. (RasADH) belongs to the protein superfamily of short-chain dehydrogenases/reductases (SDRs). As an enzyme that accepts different types of substrates--including bulky-bulky as well as small-bulky secondary alcohols or ketones--with high stereoselectivity, it offers potential
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service