Mouse, Sheep, Human, Pig
Recombinant full length ACADM (Human).
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium azide Constituents: Tris buffered saline, Whole serum, 50% Glycerol, 0.05% BSA
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Protein A purified
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/200. Predicted molecular weight: 43 kDa.
This enzyme is specific for acyl chain lengths of 4 to 16.
Lipid metabolism; mitochondrial fatty acid beta-oxidation.
Defects in ACADM are the cause of acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450]. It is an autosomal recessive disease which causes fasting hypoglycemia, hepatic dysfunction, and encephalopathy, often resulting in death in infancy.
Belongs to the acyl-CoA dehydrogenase family.
Information by UniProt
ACAD 1 antibody
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