ACADS anticorps

N° du produit ABIN7384407

L’anticorps Lapin Monoclonal anti-ACADS a été validé pour WB. Il convient pour détecter ACADS dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour ACADS anticorps (ABIN7384407)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp ACADS est non-conjugé

Application: Western Blotting (WB)

Clone: R08-4C2

Détail du produit anti-ACADS anticorps

Purification: Affinity Purified

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:1000

Restrictions: For Research Use only

Stockage

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ACADS

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

Autre désignation: ACADS

Sujet: 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.

Poids moléculaire:

Observed_MW: 44kDa

Calculated_MW: 44kDa

ID gène: 35

UniProt: P16219

Pathways: Monocarboxylic Acid Catabolic Process