ACADS Antikörper

Produktnummer ABIN7384407

Der Kaninchen Monoklonal Anti-ACADS-Antikörper wurde für WB validiert. Er ist geeignet, ACADS in Proben von Human, Maus und Ratte zu detektieren.

Kurzübersicht für ACADS Antikörper (ABIN7384407)

Target: ACADS (Acads) (Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser ACADS Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: R08-4C2

Produktdetails anti-ACADS Antikörper

Aufreinigung: Affinity Purified

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 300 μg/mL

Buffer: 50 mM Tris-Glycine( pH 7.4), 0.15M NaCl, 40 % Glycerol, 0.01 % Sodium azide and 0.05 % BSA

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ACADS

Target: ACADS (Acads) (Acyl-CoA Dehydrogenase, C-2 To C-3 Short Chain (Acads))

Andere Bezeichnung: ACADS

Hintergrund: 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,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.

Molekulargewicht:

Observed_MW: 44kDa

Calculated_MW: 44kDa

Gen-ID: 35

UniProt: P16219

Pathways: Monocarboxylic Acid Catabolic Process