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WFS1 anticorps (AA 272-876)

Cet anticorps anti-WFS1 Polyclonal Lapin (ABIN7873171) détecte spécifiquement WFS1 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7873171
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour WFS1 anticorps (AA 272-876) (ABIN7873171)

Antigène

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

Reactivité

  • 39
  • 8
  • 5
  • 3
Humain

Hôte

  • 36
  • 4
Lapin

Clonalité

  • 36
  • 4
Polyclonal

Conjugué

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp WFS1 est non-conjugé

Application

  • 33
  • 13
  • 13
  • 13
  • 9
  • 5
  • 5
  • 4
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 15
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 272-876

    Fonction

    WFS1 Antibody / Wolframin

    Purification

    Antigen affinity purified

    Immunogène

    E. coli-derived recombinant human protein (amino acids D272-K876) was used as the immunogen for the WFS1 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the WFS1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the WFS1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    WFS1 (Wolfram Syndrome 1 (WFS1))

    Autre désignation

    WFS1

    Sujet

    Wolframin is a protein that in humans is encoded by the WFS1 gene. 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.

    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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