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WFS1 anticorps

L’anticorps anti-WFS1 Polyclonal Lapin est utilisé pour la détection de WFS1 dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.
N° du produit ABIN8125758
450,00 €
Plus frais de livraison 40,00 € et TVA
50 μL
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour WFS1 anticorps (ABIN8125758)

Antigène

Voir toutes WFS1 Anticorps
WFS1 (Wolfram Syndrome 1 (WFS1))

Reactivité

  • 61
  • 14
  • 7
  • 4
Humain, Souris

Hôte

  • 58
  • 4
Lapin

Clonalité

  • 58
  • 4
Polyclonal

Conjugué

  • 22
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp WFS1 est non-conjugé

Application

  • 55
  • 32
  • 20
  • 13
  • 13
  • 13
  • 12
  • 11
  • 5
  • 3
  • 3
  • 1
Western Blotting (WB), ELISA
  • Fonction

    WFS1 Antibody

    Specificité

    WFS1 Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogène

    Synthesized peptide derived from part region of human protein

    Isotype

    IgG
  • Indications d'application

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    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/1 year

    Date de péremption

    12 months
  • Antigène

    WFS1 (Wolfram Syndrome 1 (WFS1))

    Autre désignation

    WFS1

    Sujet

    Background: This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009],

    Gene Name: WFS1

    Protein Name: Wolframin

    ID gène

    7466

    UniProt

    O76024

    Pathways

    Sensory Perception of Sound, Carbohydrate Homeostasis, ER-Nucleus Signaling, Negative Regulation of intrinsic apoptotic Signaling, SARS-CoV-2 Protein Interactome
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