Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Constituents: 2% Sucrose, PBS
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Immunogen affinity 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.
Use a concentration of 1 µg/ml. Predicted molecular weight: 44 kDa. Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T.
Lipid metabolism; mitochondrial fatty acid beta-oxidation.
Defects in ACADS are the cause of acyl-CoA dehydrogenase short-chain deficiency (ACADSD) [MIM:201470]. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.
Belongs to the acyl-CoA dehydrogenase family.
Information by UniProt
Anti-ACADS antibody 画像
Western blot - ACADS antibody (ab87544)
Anti-ACADS antibody (ab87544) 使用論文
has not yet been referenced specifically in any publications.
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