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BAAT antibody
BAAT
Reactivity: Mouse, Rat
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-BAAT Antibody
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Target
See all BAAT Antibodies
BAAT
(Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
Reactivity
All reactivities for BAAT antibodies
Mouse, Rat
Host
All hosts for BAAT antibodies
Rabbit
Clonality
All clonalities for BAAT antibodies
Polyclonal
Conjugate
All conjugates for BAAT antibodies
This BAAT antibody is un-conjugated
Application
All applications for BAAT antibodies
Western Blotting (WB)
Cross-Reactivity
Rat
Purification
Affinity purification
Immunogen
Recombinant protein corresponding to Mouse BAAT
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Discover our top product BAAT Primary Antibody
Alternatives
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Application Details
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Application Notes
WB (M,R) 1:500-1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS, pH 7.4, 0.02 % sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Target Details for BAAT
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Target
BAAT
(Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
Alternative Name
BAAT (BAAT Products )
Synonyms
BACAT antibody, BAT antibody, AI118337 antibody, AI158864 antibody, kan-1 antibody, BAAT antibody, bile acid-CoA:amino acid N-acyltransferase antibody, Bile acid-CoA:amino acid N-acyltransferase antibody, bile acid-Coenzyme A: amino acid N-acyltransferase antibody, bile acid CoA:amino acid N-acyltransferase antibody, BAAT antibody, RPIC_RS10270 antibody, Bcav_2277 antibody, Rpic12D_1765 antibody, Baat antibody, LOC481635 antibody, LOC100054567 antibody, LOC786798 antibody
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.
Molecular Weight
46 kDa
Gene ID
12012
NCBI Accession
NP_031545
UniProt
Q91X34
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