Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks and distinctive facial features similar

and distinctive facial features similar to those found in Noonan syndrome

ATP-independent protease that degrades mitochondrial transit peptides after their cleavage

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

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

This receptor is expressed preferentially in the tissues enriched in lymphocytes

Carbonyl Reductase 3 Polyclonal Antibody, 100ul Cell Culture Flasks and distinctive facial features similarCarbonyl 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.