BAAT anticorps

N° du produit ABIN7236346

Détail du produit anti-BAAT anticorps

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BAAT est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human BAAT

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:25-1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 (BAAT Produits)

Synonymes: anticorps BACAT, anticorps BAT, anticorps AI118337, anticorps AI158864, anticorps kan-1, anticorps BAAT, anticorps bile acid-CoA:amino acid N-acyltransferase, anticorps Bile acid-CoA:amino acid N-acyltransferase, anticorps bile acid-Coenzyme A: amino acid N-acyltransferase, anticorps bile acid CoA:amino acid N-acyltransferase, anticorps BAAT, anticorps RPIC_RS10270, anticorps Bcav_2277, anticorps Rpic12D_1765, anticorps Baat, anticorps LOC481635, anticorps LOC100054567, anticorps LOC786798

Sujet: 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: 46 kDa

UniProt: Q14032