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Frizzled Antikörper

Reaktivität: Human IHC (p) Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN636905
  • Target
    Frizzled
    Reaktivität
    Human
    Wirt
    Kaninchen
    Klonalität
    Polyklonal
    Applikation
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Aufreinigung
    Affinity chromatography purified
    Immunogen
    Frizzled antibody was raised in rabbit using a synthetic peptide conjugated to KLH as the immunogen.
  • Applikationshinweise
    IHC-P: 10 µg/mL
    Optimal conditions should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    Lot specific
    Buffer
    Purified by Immunoaffinity Chromatography and supplied in PBS with 0.1 % NaN3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium Azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C for short term storage. Aliquot and store at -70 °C for long term storage.
  • Target
    Frizzled
    Synonyme
    CG17697 antikoerper, CG3646 antikoerper, DFZ1 antikoerper, DFz antikoerper, DFz1 antikoerper, Dfz1 antikoerper, Dm Fz1 antikoerper, Dmel\\CG17697 antikoerper, FZ antikoerper, Frz antikoerper, Fz antikoerper, Fz1 antikoerper, frz antikoerper, fz1 antikoerper, fz[[1]] antikoerper, GLEAN_14055 antikoerper, Dvir\\GJ11377 antikoerper, GJ11377 antikoerper, dvir_GLEANR_11420 antikoerper, fz antikoerper, frizzled antikoerper, fz antikoerper, Fz antikoerper, Dvir\fz antikoerper
    Hintergrund
    Frizzled-9 is a protein that in humans is encoded by the FZD9 gene. Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.
    Pathways
    WNT Signalweg
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