ACADS antibody

Catalog No. ABIN7384407

The Rabbit Monoclonal anti-ACADS antibody has been validated for WB. It is suitable to detect ACADS in samples from Human, Mouse and Rat.

Quick Overview for ACADS antibody (ABIN7384407)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Monoclonal

Conjugate: This ACADS antibody is un-conjugated

Application: Western Blotting (WB)

Clone: R08-4C2

Product Details anti-ACADS Antibody

Purification: Affinity Purified

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:1000

Restrictions: For Research Use only

Handling

Concentration: 300 μg/mL

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for ACADS

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

Alternative Name: ACADS

Background: 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.

Molecular Weight:

Observed_MW: 44kDa

Calculated_MW: 44kDa

Gene ID: 35

UniProt: P16219

Pathways: Monocarboxylic Acid Catabolic Process