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GLUD1 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement GLUD1 dans WB, IHC et IF. Il présente une réactivité envers Humain.
N° du produit ABIN7267411

Aperçu rapide pour GLUD1 anticorps (ABIN7267411)

Antigène

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

Reactivité

  • 32
  • 17
  • 17
  • 15
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 41
  • 6
  • 1
Lapin

Clonalité

  • 41
  • 7
Monoclonal

Conjugué

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

Application

  • 34
  • 22
  • 15
  • 13
  • 13
  • 10
  • 6
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Fonction

    GLUD1 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human GLUD1

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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. [provided by RefSeq, Jan 2016],GDH, GDH1, GLUD,Amino acid metabolism,Cancer,Cell Biology & Developmental Biology,Endocrine & Metabolism,Signal Transduction,GLUD1

    Poids moléculaire

    50kDa

    ID gène

    2746

    UniProt

    P00367

    Pathways

    Positive Regulation of Peptide Hormone Secretion, L'effet Warburg
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