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Frizzled anticorps

Reactivité: Humain IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN636905
  • Antigène
    Frizzled
    Reactivité
    Humain
    Hôte
    Lapin
    Clonalité
    Polyclonal
    Application
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    Affinity chromatography purified
    Immunogène
    Frizzled antibody was raised in rabbit using a synthetic peptide conjugated to KLH as the immunogen.
  • Indications d'application
    IHC-P: 10 µg/mL
    Optimal conditions should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    Lot specific
    Buffer
    Purified by Immunoaffinity Chromatography and supplied in PBS with 0.1 % NaN3.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium Azide: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C for short term storage. Aliquot and store at -70 °C for long term storage.
  • Antigène
    Frizzled
    Synonymes
    anticorps CG17697, anticorps CG3646, anticorps DFZ1, anticorps DFz, anticorps DFz1, anticorps Dfz1, anticorps Dm Fz1, anticorps Dmel\\CG17697, anticorps FZ, anticorps Frz, anticorps Fz, anticorps Fz1, anticorps frz, anticorps fz1, anticorps fz[[1]], anticorps GLEAN_14055, anticorps Dvir\\GJ11377, anticorps GJ11377, anticorps dvir_GLEANR_11420, anticorps fz, anticorps frizzled, anticorps fz, anticorps Fz, anticorps Dvir\fz
    Sujet
    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
    Signalisation WNT
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