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

ZBTB20 anticorps

Cet anticorps anti-ZBTB20 est un anticorps Lapin Polyclonal détectant ZBTB20 dans WB. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7012097

Aperçu rapide pour ZBTB20 anticorps (ABIN7012097)

Antigène

Voir toutes ZBTB20 Anticorps
ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))

Reactivité

  • 12
  • 6
  • 5
  • 5
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 12
  • 1
Lapin

Clonalité

  • 12
  • 1
Polyclonal

Conjugué

  • 13
Cet anticorp ZBTB20 est non-conjugé

Application

  • 10
  • 5
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human ZBTB20 (NP_056457.3).

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000

    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

    ZBTB20 (Zinc Finger and BTB Domain Containing 20 (ZBTB20))

    Autre désignation

    ZBTB20

    Sujet

    This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Poids moléculaire

    Observed_MW: 81 kDa

    Calculated_MW: 73 kDa/81 kDa

    ID gène

    26137

    UniProt

    Q9HC78
Vous êtes ici:
Chat with us!