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FACS analysis of HeLa cells using GTX83320 Wnt1 antibody [10C8]. Green : Wnt1 Purple : negative control
FACS analysis of HeLa cells using GTX83320 Wnt1 antibody [10C8]. Green : Wnt1 Purple : negative control
FACS analysis of HeLa cells using GTX83320 Wnt1 antibody [10C8]. Green : Wnt1 Purple : negative control

Wnt1 antibody [10C8]

GTX83320
GeneTex
ApplicationsFlow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetWNT1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Wnt1 antibody [10C8]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1/500 - 1/2000. ICC/IF: 1/200 - 1/1000. IHC-P: 1/200 - 1/1000. FACS: 1/200 - 1/400. ELISA: 1/10000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    10C8
  • Conjugate
    Unconjugated
  • Gene ID7471
  • Target name
    WNT1
  • Target description
    Wnt family member 1
  • Target synonyms
    BMND16; INT1; OI15; proto-oncogene Int-1 homolog; proto-oncogene Wnt-1; wingless-type MMTV integration site family member 1; wingless-type MMTV integration site family, member 1 (oncogene INT1)
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP04628
  • Protein Name
    Proto-oncogene Wnt-1
  • 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 is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV. Vollersen N et al., 2021 Nov 10, Bone Res
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