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

RFX6 anticorps

L’anticorps Lapin Polyclonal anti-RFX6 a été validé pour ELISA et IHC. Il convient pour détecter RFX6 dans des échantillons de Humain et Souris.
N° du produit ABIN7246697

Aperçu rapide pour RFX6 anticorps (ABIN7246697)

Antigène

Voir toutes RFX6 Anticorps
RFX6 (Regulatory Factor X 6 (RFX6))

Reactivité

  • 19
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 17
  • 2
Lapin

Clonalité

  • 19
Polyclonal

Conjugué

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RFX6 est non-conjugé

Application

  • 6
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human RFX6

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.96 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

    RFX6 (Regulatory Factor X 6 (RFX6))

    Autre désignation

    RFX6

    Sujet

    The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.

    UniProt

    Q8HWS3

    Pathways

    Carbohydrate Homeostasis
Vous êtes ici:
Chat with us!