Bile acid-CoA:amino acid N-acyltransferase

BT-AP06643

Rabbit

IgG

20ul,50ul,100ul

Polyclonal

Synthesized peptide derived from part region of human protein

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

1 mg/ml

Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

-20°C for 1 year

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.

Human: Q14032; Mouse: Q91X34; Rat: Q63276;

Human: 570

Bile acid-CoA:amino acid N-acyltransferase ;BACAT;BAT;EC 2.3.1.65;Glycine N-choloyltransferase;Long-chain fatty-acyl-CoA hydrolase;EC 3.1.2.2

Cancer; Metabolism; Signal transduction

BAAT