ACOX2 (Human) polyclonal, anti-human

Background:
The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children.

Other Names:
Peroxisomal acyl-coenzyme A oxidase 2, 1.17.99.3, 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase, 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase, Trihydroxycoprostanoyl-CoA oxidase, THCA-CoA oxidase, THCCox, ACOX2

Antigen Types:
Synthetic Peptide

Gene Name:
ACOX2 (HGNC:120)
Gene ID:
8309
Primary Accession: Q99424
Other Accession: NP_003491;8309;