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Anti-FZD9 Rabbit Polyclonal Antibody
Anti-FZD9 Rabbit Polyclonal Antibody
Catalog #: 10108-498
Supplier:  Prosci
FZD9 antibody
Anti-FZD9 Rabbit Polyclonal Antibody
Catalog #: 10108-498
Supplier:  Prosci
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    frizzled class receptor 9
  • Clonality:
    Polyclonal
  • Gene ID:
    O00144
  • Host:
    Rabbit
  • Reactivity:
    Human,
    Dog
  • Antigen symbol:
    FZD9
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • ImmunoChemistry:
    Yes
  • Size:
    100 ul
  • Western blot:
    Yes
  • Form:
    Liquid
  • Antigen synonyms:
    FZD9
  • Storage buffer:
    Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
  • Molecular weight:
    65 kDa
  • Storage temperature:
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FZD9 antibody at –20 °C. As with any antibody avoid repeat freeze-thaw cycles.
  • Shipping temperature:
    4 °C
  • Immunogen:
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FZD9.
  • Purification:
    Antibody is purified by protein A chromatography method.
  • Cat. no.:
    10108-498
  • Supplier No.:
    29-541

Specifications

About this item

FZD9 contains 1 FZ (frizzled) domain and belongs to the G-protein coupled receptor Fz/Smo family. It is receptor for Wnt proteins. Most of frizzled receptors are coupled to the beta-catenin canonical signaling pathway, which leads to the activation of disheveled proteins, inhibition of GSK-3 kinase, nuclear accumulation of beta-catenin and activation of Wnt target genes. A second signaling pathway involving PKC and calcium fluxes has been seen for some family members. It may be involved in transduction and intercellular transmission of polarity information during tissue morphogenesis and/or in differentiated tissues. 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.

FZD9 antibody can be used for detection of FZD9 by ELISA at 1:1562500. FZD9 antibody can be used for detection of FZD9 by western blot at 2.5 ?g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Antibody is purified by protein A chromatography method.

Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Type: Primary
Antigen: FZD9
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype:
Reactivity: Human, Dog

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