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WWOX Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch WWOX in WB, ELISA und IHC (p). Er zeigt eine Reaktivität gegenüber Human, Maus und Ratte.
Produktnummer ABIN5708495

Kurzübersicht für WWOX Antikörper (ABIN5708495)

Target

Alle WWOX Antikörper anzeigen
WWOX (WW Domain Containing Oxidoreductase (WWOX))

Reaktivität

  • 58
  • 41
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 62
  • 3
  • 2
Kaninchen

Klonalität

  • 65
  • 2
Polyklonal

Konjugat

  • 44
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser WWOX Antikörper ist unkonjugiert

Applikation

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

    Antigen affinity purified

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

    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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    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))

    Andere Bezeichnung

    WWOX

    Hintergrund

    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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