Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks The variation of this locus

The variation of this locus may affect the development of alcohol-related problems

The protein encoded by this gene resides in the mitochondria| and is essential for SDH assembly| but does not physically associate with the complex in vivo

and distinctive facial features similar to those found in Noonan syndrome

Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency

Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks The variation of this locusCarbonyl reductase 3 catalyzes the reduction of a large number of biologically and pharmacologically active carbonyl compounds to their corresponding alcohols. The enzyme is classified as a monomeric NADPH dependent oxidoreductase. CBR3 contains three exons spanning 11. 2 kilobases and is closely linked to another carbonyl reductase gene CBR1.