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The image on the left is immunohistochemistry of paraffin-embedded Human colon cancer tissue using CSB-PA194965(BAAT Antibody) at dilution 1/30, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human colon cancer tissue using CSB-PA194965(BAAT Antibody) at dilution 1/30, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human colon cancer tissue using CSB-PA194965(BAAT Antibody) at dilution 1/30, on the right is treated with fusion protein. (Original magnification: x200)

BAAT Antibody

CSB-PA194965
Cusabio
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse
TargetBAAT
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Overview

  • Supplier
    Cusabio
  • Product Name
    BAAT Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID570
  • Target name
    BAAT
  • Target description
    bile acid-CoA:amino acid N-acyltransferase
  • Target synonyms
    BACAT, BACD1, BAT, FHCA3, HCHO, bile acid-CoA:amino acid N-acyltransferase, bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase), bile acid Coenzyme A: amino acid N-acyltransferase (glycine N-choloyltransferase), bile acid-CoA thioesterase, choloyl-CoA hydrolase, long-chain fatty-acyl-CoA hydrolase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ14032
  • Protein Name
    Bile acid-CoA:amino acid N-acyltransferase
  • Scientific Description
    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.
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161