This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family.
The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway.
Its enzymatic activity is highest with medium-chain-length fatty acids.
Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia.
The human genome contains a related pseudogene.
Applications:Suitable for use in Western Blot.
Other applications not tested.
Recommended Dilution:Optimal dilutions to be determined by the researcher.