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ICC/IF analysis of PFA-fixed HeLa cells using GTX04615 SLC25A5 antibody. Red : Primary antibody Green : Beta tubulin Blue : DAPI Permeabilization : 0.1% Triton X-100
ICC/IF analysis of PFA-fixed HeLa cells using GTX04615 SLC25A5 antibody. Red : Primary antibody Green : Beta tubulin Blue : DAPI Permeabilization : 0.1% Triton X-100
ICC/IF analysis of PFA-fixed HeLa cells using GTX04615 SLC25A5 antibody. Red : Primary antibody Green : Beta tubulin Blue : DAPI Permeabilization : 0.1% Triton X-100

SLC26A5 antibody

GTX04615
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
TargetSLC26A5
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Overview

  • Supplier
    GeneTex
  • Product Name
    SLC26A5 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:1000-1:3000. ICC/IF: 1:100-1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID375611
  • Target name
    SLC26A5
  • Target description
    solute carrier family 26 member 5
  • Target synonyms
    DFNB61; PRES; prestin; prestin (motor protein); solute carrier family 26 (anion exchanger), member 5
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP58743
  • Protein Name
    Prestin
  • Scientific Description
    This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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