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HOXD10 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement HOXD10 dans IF. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7263687

Aperçu rapide pour HOXD10 anticorps (ABIN7263687)

Antigène

Voir toutes HOXD10 Anticorps
HOXD10 (Homeobox D10 (HOXD10))

Reactivité

  • 37
  • 26
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 40
  • 2
  • 1
Lapin

Clonalité

  • 41
  • 2
Polyclonal

Conjugué

  • 24
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp HOXD10 est non-conjugé

Application

  • 31
  • 21
  • 12
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human HOXD10 (NP_002139.2).

    Isotype

    IgG
  • Indications d'application

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    HOXD10 (Homeobox D10 (HOXD10))

    Autre désignation

    HOXD10

    Sujet

    This gene is a member of the Abd-B homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox D genes located on chromosome 2. The encoded nuclear protein functions as a sequence-specific transcription factor that is expressed in the developing limb buds and is involved in differentiation and limb development. Mutations in this gene have been associated with Wilm's tumor and congenital vertical talus (also known as 'rocker-bottom foot' deformity or congenital convex pes valgus) and/or a foot deformity resembling that seen in Charcot-Marie-Tooth disease.

    ID gène

    3236

    UniProt

    P28358
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