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FZD9 antibody (3rd Extracellular Domain)

This anti-FZD9 antibody is a Rabbit Polyclonal antibody detecting FZD9 in ELISA and IHC. Suitable for Human and Gibbon.
Catalog No. ABIN2469414

Quick Overview for FZD9 antibody (3rd Extracellular Domain) (ABIN2469414)

Target

See all FZD9 Antibodies
FZD9 (Frizzled Family Receptor 9 (FZD9))

Reactivity

  • 59
  • 28
  • 20
  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Gibbon

Host

  • 57
  • 1
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Rabbit

Clonality

  • 57
  • 2
Polyclonal

Conjugate

  • 43
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FZD9 antibody is un-conjugated

Application

  • 35
  • 32
  • 16
  • 10
  • 9
  • 7
  • 2
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Binding Specificity

    • 11
    • 9
    • 7
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    3rd Extracellular Domain

    Specificity

    BLAST analysis of the peptide immunogen showed no homology with other human proteins, except FZD10 (47 % ).

    Purification

    Immunoaffinity Chromatography

    Immunogen

    Frizzled 9 antibody was raised against a peptide located in the 3rd extracellular domain of Frizzled 9 (Human).
  • Application Notes

    Frizzled 9 antibody can be used in immunohistochemistry starting at 15 - 20 μg/mL.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS, 0.1 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    As with all antibodies avoid freeze/thaw cycles.

    Storage

    4 °C/-80 °C

    Storage Comment

    Frizzled 9 antibody should be stored long term (months) at -80 °C and short term (days) at 4 °C.
  • Target

    FZD9 (Frizzled Family Receptor 9 (FZD9))

    Alternative Name

    Frizzled 9

    Background

    FZD9, previously named frizzled-3, is a Frizzled Receptor that mediates Wnt signaling. It may contribute to the Williams-Beuren syndrome described as supravalvular and aortic stenosis, and to infantile hypercalcemia.

    Gene ID

    8326

    UniProt

    O00144

    Pathways

    WNT Signaling
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