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WDR4 anticorps

Cet anticorps anti-WDR4 est un anticorps Lapin Monoclonal détectant WDR4 dans WB et IHC. Adapté pour Humain.
N° du produit ABIN7271355

Aperçu rapide pour WDR4 anticorps (ABIN7271355)

Antigène

Voir toutes WDR4 Anticorps
WDR4 (WD Repeat Domain 4 (WDR4))

Reactivité

  • 33
  • 13
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 31
  • 2
Lapin

Clonalité

  • 30
  • 3
Monoclonal

Conjugué

  • 21
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp WDR4 est non-conjugé

Application

  • 25
  • 11
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Fonction

    WDR4 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human WDR4

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    WDR4 (WD Repeat Domain 4 (WDR4))

    Autre désignation

    WDR4

    Sujet

    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012],TRM82, TRMT82,Epigenetics & Nuclear Signaling,WDR4

    Poids moléculaire

    45kDa

    ID gène

    10785

    UniProt

    P57081
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