BAAT (Human) Recombinant Protein (Q01)

Catalog # H00000570-Q01

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Size:25 ug
Price: USD $ 510.00
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Size:10 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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  • Specification

    Product Description

    Human BAAT partial ORF ( NP_001692, 258 a.a. - 355 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    NGTNFPFGIPQVYHGQIHQPLPHSAQLISTNALGLLELYRTFETTQVGASQYLFPIEEAQGQFLFIVGEGDKTINSKAHAEQAIGQLKRHGKNNWTLL

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    36.52

    Interspecies Antigen Sequence

    Mouse (58); Rat (59)

    Preparation Method

    in vitro wheat germ expression system

    Purification

    Glutathione Sepharose 4 Fast Flow

    Quality Control Testing

    12.5% SDS-PAGE Stained with Coomassie Blue.

    Storage Buffer

    50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

    Note

    Best use within three months from the date of receipt of this protein.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — BAAT

    Entrez GeneID

    570

    GeneBank Accession#

    NM_001701

    Protein Accession#

    NP_001692

    Gene Name

    BAAT

    Gene Alias

    BACAT, BAT, FLJ20300, MGC104432

    Gene Description

    bile acid Coenzyme A: amino acid N-acyltransferase (glycine N-choloyltransferase)

    Omim ID

    602938 607748

    Gene Ontology

    Hyperlink

    Gene Summary

    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. [provided by RefSeq

    Other Designations

    OTTHUMP00000021802|bile acid Coenzyme A: amino acid N-acyltransferase|glycine N-choloyltransferase

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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