ACADM Antilichaam

This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

34

P11310

Human, Mouse

Recombinant fusion protein containing a sequence corresponding to amino acids 26-421 of human ACADM (NP_000007.1) .

Unconjugated

Primary Antibodies

Cancer, Signal Transduction

Affinity purification

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

IgG

ACADM

Acyl-CoA dehydrogenase, C-4 to C-12 straight chain

Homo sapiens

ACADM, ACAD1, MCAD, MCADH

WB, IHC

Liquid