Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

WWOX anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement WWOX dans WB, ELISA et IHC (p). Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN5708495

Aperçu rapide pour WWOX anticorps (ABIN5708495)

Antigène

Voir toutes WWOX Anticorps
WWOX (WW Domain Containing Oxidoreductase (WWOX))

Reactivité

  • 55
  • 39
  • 11
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 59
  • 3
  • 2
Lapin

Clonalité

  • 62
  • 2
Polyclonal

Conjugué

  • 41
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp WWOX est non-conjugé

Application

  • 44
  • 23
  • 15
  • 11
  • 6
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Purification

    Antigen affinity purified

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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

    Stock

    -20 °C

    Stockage commentaire

    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.
  • Antigène

    WWOX (WW Domain Containing Oxidoreductase (WWOX))

    Autre désignation

    WWOX

    Sujet

    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
Vous êtes ici:
Chat with us!