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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   BAAT Antibody (monoclonal) (M02)   

BAAT Antibody (monoclonal) (M02)

Mouse monoclonal antibody raised against a partial recombinant BAAT.

  • WB - BAAT Antibody (monoclonal) (M02) AT1257a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.52 KDa) .
  • WB - BAAT Antibody (monoclonal) (M02) AT1257a
    BAAT monoclonal antibody (M02), clone 5B6 Western Blot analysis of BAAT expression in HepG2 ( (Cat # AT1257a )
  • E - BAAT Antibody (monoclonal) (M02) AT1257a
    Detection limit for recombinant GST tagged BAAT is approximately 0.3ng/ml as a capture antibody.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q14032
Other Accession NM_001701
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG1 Kappa
Clone Names 5B6
Calculated MW 46299 Da
Additional Information
Gene ID 570
Other Names Bile acid-CoA:amino acid N-acyltransferase, BACAT, BAT, Glycine N-choloyltransferase, Long-chain fatty-acyl-CoA hydrolase, BAAT
Target/Specificity BAAT (NP_001692, 258 a.a. ~ 355 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsBAAT Antibody (monoclonal) (M02) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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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.


An approach based on a genome-wide association study reveals candidate loci for narcolepsy. Shimada M, et al. Hum Genet, 2010 Oct. PMID 20677014.High-resolution mass spectrometry analysis of protein oxidations and resultant loss of function. Barnes S, et al. Biochem Soc Trans, 2008 Oct. PMID 18793185.Genetic polymorphism of bile acid CoA: amino acid N-acyltransferase in Japanese individuals. Tougou K, et al. Drug Metab Pharmacokinet, 2007 Apr. PMID 17495420.Human and rat bile acid-CoA:amino acid N-acyltransferase are liver-specific peroxisomal enzymes: implications for intracellular bile salt transport. Pellicoro A, et al. Hepatology, 2007 Feb. PMID 17256745.Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags. Wang AG, et al. Biochem Biophys Res Commun, 2006 Jul 7. PMID 16712791.

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$ 315.00
Cat# AT1257a
(40 western blots)
Availability: 7-10 days
Bulk Size
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