Involvement in diseaseDefects 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.
Sequence similaritiesBelongs to the acyl-CoA dehydrogenase family.
All lanes : Anti-ACADS antibody (ab72767) at 1/500 dilution
Lane 1 : Transfected 293T cell lysate Lane 2 : Non-transfected 293T cell lysate
Lysates/proteins at 25 µg per lane.
Secondary Goat Anti-Mouse IgG (H&L)-HRP conjugated at 1/2500 dilution
Predicted band size : 44 kDa Observed band size : 44 kDa Additional bands at : 42 kDa. We are unsure as to the identity of these extra bands.
References for Anti-ACADS antibody (ab72767)
This product has been referenced in:
Cornelius N et al. Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblasts. Hum Mol GenetN/A:N/A (2014).
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