BAAT anticorps

N° du produit ABIN6571255

Cet anticorps anti-BAAT est un anticorps Lapin Polyclonal détectant BAAT dans WB. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour BAAT anticorps (ABIN6571255)

Antigène: BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BAAT est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-BAAT anticorps

Purification: Affinity purification

Immunogène: Recombinant protein of human BAAT

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

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 BAAT

Antigène: BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))

Autre désignation: BAAT

Sujet:

Synonyms: FLJ20300,BAAT,BAAT,BACAT,BAT,Bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase),Bile acid CoA:amino acid N acyltransferase,Bile acid Coenzyme A amino acid N acyltransferase glycine N choloyltransferase,Bile acid Coenzyme A: amino acid N acyltransferase,Bile acid-CoA:amino acid N-acyltransferase,Glycine N choloyltransferase,Glycine N-choloyltransferase,Long chain fatty acyl CoA hydrolase,Long-chain fatty-acyl-CoA hydrolase,MGC104432

Background: The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene.

Poids moléculaire:

Observed_MW: 46kDa

Calculated_MW: 46kDa

ID gène: 570

UniProt: Q14032