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ProductsBack/OATP8 antibody, Internal
FACS analysis of PFA-fixed HepG2 cells using GTX88295 OATP8 antibody, Internal. Blue : Primary antibody Black : IgG control Permeabilization : 0.5% Triton Dilution : 10microg/ml
FACS analysis of PFA-fixed HepG2 cells using GTX88295 OATP8 antibody, Internal. Blue : Primary antibody Black : IgG control Permeabilization : 0.5% Triton Dilution : 10microg/ml
FACS analysis of PFA-fixed HepG2 cells using GTX88295 OATP8 antibody, Internal. Blue : Primary antibody Black : IgG control Permeabilization : 0.5% Triton Dilution : 10microg/ml

OATP8 antibody, Internal

GTX88295
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
DownloadDatasheet
Product group Antibodies
ReactivityHuman
TargetSLCO1B3
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Overview

  • Supplier
    GeneTex
  • Product Name
    OATP8 antibody, Internal
  • Delivery Days Customer
    9
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID28234
  • Target name
    SLCO1B3
  • Target description
    solute carrier organic anion transporter family member 1B3
  • Target synonyms
    HBLRR; liver-specific organic anion transporter 2; liver-specific organic anion transporter 3TM13; LST-2; LST3; LST-3TM13; OATP1B3; OATP8; OATP-8; organic anion transporter 8; organic anion transporter LST-3c; organic anion-transporting polypeptide 8; SLC21A8; solute carrier family 21 (organic anion transporter), member 8; solute carrier organic anion transporter family member 1B3
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ9NPD5
  • Protein Name
    Solute carrier organic anion transporter family member 1B3
  • Scientific Description
    This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of endogenous and xenobiotic compounds and plays a critical role in bile acid and bilirubin transport. Mutations in this gene are a cause of Rotor type hyperbilirubinemia. Alternative splicing of this gene and the use of alternative promoters results in transcript variants encoding different isoforms that differ in their tissue specificity. [provided by RefSeq, Mar 2017]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203