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ICC/IF analysis of PC12 cells using GTX83127 WNT5A antibody [6F2]. Green : WNT5A Blue: DRAQ5 fluorescent DNA dye
ICC/IF analysis of PC12 cells using GTX83127 WNT5A antibody [6F2]. Green : WNT5A Blue: DRAQ5 fluorescent DNA dye
ICC/IF analysis of PC12 cells using GTX83127 WNT5A antibody [6F2]. Green : WNT5A Blue: DRAQ5 fluorescent DNA dye

Wnt5a antibody [6F2]

GTX83127
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetWNT5A
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Overview

  • Supplier
    GeneTex
  • Product Name
    Wnt5a antibody [6F2]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1/500 - 1/2000. ICC/IF: 1/200 - 1/1000. IHC-P: 1/200 - 1/1000. ELISA: 1/10000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    6F2
  • Conjugate
    Unconjugated
  • Gene ID7474
  • Target name
    WNT5A
  • Target description
    Wnt family member 5A
  • Target synonyms
    hWNT5A, protein Wnt-5a, WNT-5A protein, epididymis secretory sperm binding protein, wingless-type MMTV integration site family, member 5A
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP41221
  • Protein Name
    Protein Wnt-5a
  • Scientific Description
    The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene encodes a member of the WNT family that signals through both the canonical and non-canonical WNT pathways. This protein is a ligand for the seven transmembrane receptor frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203