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GLUD1 / GLUD2 (AA 54-553) anticorps (HRP)

L’anticorps anti-GLUD1 / GLUD2 Polyclonal Lapin est utilisé pour la détection de GLUD1 / GLUD2 dans des échantillons de Humain, Souris et Rat. Il a été validé pour ELISA, WB et IHC.
N° du produit ABIN7993582
720,50 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour GLUD1 / GLUD2 (AA 54-553) anticorps (HRP) (ABIN7993582)

Antigène

GLUD1 / GLUD2

Reactivité

Humain, Souris, Rat

Hôte

  • 12
  • 1
Lapin

Clonalité

  • 13
Polyclonal

Conjugué

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
HRP

Application

  • 11
  • 5
  • 5
  • 4
  • 4
  • 2
  • 1
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 12
    • 1
    AA 54-553

    Fonction

    Anti-GLUD1/2 Antibody HRP Conjugated

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human GLUD1/2 recombinant protein (Position: S54-A553).

    Isotype

    IgG
  • Indications d'application

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    Stock

    -20 °C

    Stockage commentaire

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    Date de péremption

    12 months
  • Antigène

    GLUD1 / GLUD2

    Autre désignation

    GLUD1/2

    Sujet

    Background: This gene encodes glutamate dehydrogenase, which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha-ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid-induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in multiple transcript variants. The related glutamate dehydrogenase 2 gene on the human X-chromosome originated from this gene via retrotransposition and encodes a soluble form of glutamate dehydrogenase. Related pseudogenes have been identified on chromosomes 10, 18 and X.

    Gene Full Name: glutamate dehydrogenase 1/2

    ID gène

    2746, 2747

    UniProt

    P00367
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