BAAT Antikörper

Produktnummer ABIN7236346

Produktdetails anti-BAAT Antikörper

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

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BAAT Antikörper ist unkonjugiert

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

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human BAAT

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:25-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.4 mg/mL

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

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 BAAT

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

Andere Bezeichnung: BAAT (BAAT Produkte)

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

Hintergrund: 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.

Molekulargewicht: 46 kDa

UniProt: Q14032