BAAT Antikörper

Produktnummer ABIN6571255

Dieser Anti-BAAT-Antikörper ist ein Kaninchen-Polyklonal-Antikörper zum Nachweis von BAAT in WB. Geeignet für Human, Maus und Ratte.

Kurzübersicht für BAAT Antikörper (ABIN6571255)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BAAT Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-BAAT Antikörper

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human BAAT

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

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

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

Hintergrund:

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.

Molekulargewicht:

Observed_MW: 46kDa

Calculated_MW: 46kDa

Gen-ID: 570

UniProt: Q14032