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.
仕様
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
Host：Rabbit
Reactivity：Human
Applications：WB,IHC,ELISA
Concentration：0.4mg/mL
Immunogen：Recombinant protein of human BAAT
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
Dilution：WB 1：500-1：2000, IHC 1：25-1：100
Swissprot：Q14032
Isotype：IgG
Research Areas：Cancer, Metabolism, Signal transduction
