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IHC-P analysis of human small intestine using GTX47585 ASBT antibody, C-term. Antigen retrieval : citrate buffer pH 6 Dilution : 3.8microg/ml
IHC-P analysis of human small intestine using GTX47585 ASBT antibody, C-term. Antigen retrieval : citrate buffer pH 6 Dilution : 3.8microg/ml
IHC-P analysis of human small intestine using GTX47585 ASBT antibody, C-term. Antigen retrieval : citrate buffer pH 6 Dilution : 3.8microg/ml

ASBT antibody, C-term

GTX47585
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
DownloadDatasheet
Product group Antibodies
ReactivityHuman
TargetSLC10A2
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Overview

  • Supplier
    GeneTex
  • Product Name
    ASBT antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 3-6microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID6555
  • Target name
    SLC10A2
  • Target description
    solute carrier family 10 member 2
  • Target synonyms
    ASBT; IBAT; ileal apical sodium-dependent bile acid transporter; ileal sodium/bile acid cotransporter; ileal sodium-dependent bile acid transporter; ISBT; Na(+)-dependent ileal bile acid transporter; NTCP2; PBAM; PBAM1; sodium/taurocholate cotransporting polypeptide, ileal; solute carrier family 10 (sodium/bile acid cotransporter family), member 2; solute carrier family 10 (sodium/bile acid cotransporter), member 2
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ12908
  • Protein Name
    Ileal sodium/bile acid cotransporter
  • Scientific Description
    This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also critical for cholesterol homeostasis. Mutations in this gene cause primary bile acid malabsorption (PBAM); muatations in this gene may also be associated with other diseases of the liver and intestines, such as familial hypertriglyceridemia (FHTG). [provided by RefSeq, Mar 2010]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203