ACAD-9 Polyclonal Antibody

Background:
acyl-CoA dehydrogenase family member 9(ACAD9) Homo sapiens This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010],

Alternative Names:
ACAD9, Acyl-CoA dehydrogenase family member 9, mitochondrial, ACAD-9

Immunogen: Synthesized peptide derived from ACAD-9 . at AA range: 530-610

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

GeneID: ACAD9

Storage: -20°C/1 year

NOTE: For Research Use Only