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OVOL2 anticorps

Cet anticorps anti-OVOL2 est un anticorps Lapin Polyclonal détectant OVOL2 dans WB, ELISA et IHC. Adapté pour Humain et Souris.
N° du produit ABIN7246562

Aperçu rapide pour OVOL2 anticorps (ABIN7246562)

Antigène

Voir toutes OVOL2 Anticorps
OVOL2 (Ovo-Like 2 (OVOL2))

Reactivité

  • 28
  • 23
  • 19
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 36
  • 3
Lapin

Clonalité

  • 38
  • 1
Polyclonal

Conjugué

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp OVOL2 est non-conjugé

Application

  • 27
  • 13
  • 13
  • 10
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human OVOL2

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.84 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    OVOL2 (Ovo-Like 2 (OVOL2))

    Autre désignation

    OVOL2

    Sujet

    This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 30 kDa

    UniProt

    Q9BRP0

    Pathways

    Tube Formation
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