BAAT Polyclonal Antibody

Rabbit Anti-BAAT Polyclonal Antibody

Product Specifications

Background

The Bile Acid-CoA: amino Acid N-Acyltransferase encoded by BAAT 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.

CAS Number

9007-83-4

Product Name Alternative

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

Gene ID

570

Accession Number

Q14032

Reactivity

Human, Rat, Mouse

Immunogen

Synthesized peptide derived from part region of human BAAT protein

Clonality

Polyclonal

Tag

BAAT

Applications

WB, ELISA

Purification Method

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

Concentration

1 mg/ml

Molecular Weight

45kD

Precautions

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Shipping Conditions

Gel pack with blue ice.

Storage Conditions

Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Notes

The antibody detects endogenous levels of BAAT protein

Formulation

Liquid solution

Buffer pH

PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

Applications Notes

Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000; ELISA 1:5000-20000