BAAT antibody

Catalog No. ABIN6571255

The Rabbit Polyclonal anti-BAAT antibody (ABIN6571255) specifically detects BAAT in WB. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for BAAT antibody (ABIN6571255)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BAAT antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-BAAT Antibody

Purification: Affinity purification

Immunogen: Recombinant protein of human BAAT

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000

Restrictions: For Research Use only

Handling

Concentration: 1 mg/mL

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

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

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for BAAT

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

Alternative Name: BAAT

Background:

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.

Molecular Weight:

Observed_MW: 46kDa

Calculated_MW: 46kDa

Gene ID: 570

UniProt: Q14032