Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks retinoic acid receptor alpha

retinoic acid receptor alpha

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

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

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

This gene and related family members AQP0

Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks retinoic acid receptor alphaCarbonyl 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.