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alpha KGDHC anticorps

Cet anticorps anti-alpha KGDHC est un anticorps Lapin Polyclonal détectant alpha KGDHC dans WB, IHC et IF. Adapté pour Humain, Rat et Souris.
N° du produit ABIN7011083

Aperçu rapide pour alpha KGDHC anticorps (ABIN7011083)

Antigène

Voir toutes alpha KGDHC (alphaKGDHC) Anticorps
alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))

Reactivité

  • 29
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 28
  • 3
Lapin

Clonalité

  • 28
  • 3
Polyclonal

Conjugué

  • 20
  • 3
  • 3
  • 3
  • 1
  • 1
Cet anticorp alpha KGDHC est non-conjugé

Application

  • 27
  • 18
  • 15
  • 7
  • 6
  • 5
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human OGDH (NP_001003941.1).

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000 IHC 1:50-1:200 IF 1:10-1:100

    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

    alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))

    Autre désignation

    OGDH

    Sujet

    This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    Poids moléculaire

    Observed_MW: 116 kDa

    Calculated_MW: 48 kDa/115 kDa

    ID gène

    4967

    UniProt

    Q02218
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