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

GLUD1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement GLUD1 dans IHC et IF. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7263621

Aperçu rapide pour GLUD1 anticorps (ABIN7263621)

Antigène

Voir toutes GLUD1 Anticorps
GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

Reactivité

  • 32
  • 16
  • 16
  • 15
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 41
  • 6
  • 1
Lapin

Clonalité

  • 40
  • 8
Polyclonal

Conjugué

  • 32
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GLUD1 est non-conjugé

Application

  • 35
  • 22
  • 15
  • 13
  • 13
  • 10
  • 6
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human GLUD1 (NP_005262.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:100-1:200 IF 1:50-1:200

    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

    GLUD1 (Glutamate Dehydrogenase 1 (GLUD1))

    Autre désignation

    GLUD1

    Sujet

    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.

    ID gène

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, L'effet Warburg
Vous êtes ici:
Chat with us!