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WWOX antibody

This Rabbit Polyclonal antibody specifically detects WWOX in WB, ELISA and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN5708495

Quick Overview for WWOX antibody (ABIN5708495)

Target

See all WWOX Antibodies
WWOX (WW Domain Containing Oxidoreductase (WWOX))

Reactivity

  • 58
  • 41
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 62
  • 3
  • 2
Rabbit

Clonality

  • 65
  • 2
Polyclonal

Conjugate

  • 44
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This WWOX antibody is un-conjugated

Application

  • 47
  • 26
  • 16
  • 13
  • 7
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Purification

    Antigen affinity purified

    Immunogen

    A recombinant human protein corresponding to amino acids M1-D245 was used as the immunogen for the WWOX antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the WWOX antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL, IHC (FFPE): 1-2 μg/mL, Direct ELISA: 0.1-0.5 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the WWOX antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    WWOX (WW Domain Containing Oxidoreductase (WWOX))

    Alternative Name

    WWOX

    Background

    WW domain-containing oxidoreductase is an enzyme that in humans is encoded by the WWOX gene. This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. It spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9NZC7
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