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.

Classification:

Primary antibody

Alternative names:

Peroxisomal acyl-coenzyme A oxidase 2 ;EC 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

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human protein . at AA range: 270-350

Concentration:

1 mg/ml

Molecular weight:

Applications:

WB, ELISA

Storage:

-20°C for 1 year

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