This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. It is an autosomal recessive disorder resulting in acute acidosis and muscle weakness in infants, and a form of lipid-storage myopathy in adults.

Dettagli prodotto

• Codice: E-AB-81522_100μL
• Marca: Elabscience
• Specie target: Human;Mouse;Rat
• Host: Rabbit
• Concentrazione: 300 μg/mL
• Link: Apri link
• Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
• Isotipo: IgG
• Clonalità: Rabbit Monoclonal
• Clone: R08-4C2
• Coniugazione: Unconjugated
• Applicazione: WB
• Diluizione: WB 1:500-1:1000
• Simbolo target: ACADS
• Ig target: ACAD3;ACADS;ACADS;Acyl Coenzyme A dehydrogenase;C2 to C3 short chain;Acyl-CoA dehydrogenase;C2 to C3 short chain;Acyl-CoA dehydrogenase;short chain;Acyl-Coenzyme A dehydrogenase;short chain;AI196007;Bcd-1;Bcd1;Butyryl CoA dehydrogenase;Butyryl-CoA dehydrogenase;EC 1.3.99.2;mitochondrial;SCAD;Short chain acyl CoA dehydrogenase;Short-chain specific acyl-CoA dehydrogenase;Short-chain specific acyl-CoA dehydrogenase;mitochondrial;Unsaturated acyl CoA reductase
• Area di ricerca: Cancer;Cardiovascular;Metabolism;Signal Transduction