Background:

The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family| which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency| leading to nonketotic hypoglycemia.

Classification:

Primary antibody

Alternative names:

ACADL

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human ACADL

Concentration:

1 mg/ml

Molecular weight:

47300

Applications:

WB

Storage:

-20°C for 1 year

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