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alpha KGDHC anticorps
alphaKGDHC
Reactivité: Humain, Souris, Rat
WB, IHC, IF
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN6292773
Détail du produit anti-alpha KGDHC anticorps
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Antigène
Voir toutes alpha KGDHC (alphaKGDHC) Anticorps
alpha KGDHC (alphaKGDHC)
(alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
Reactivité
Toutes les réactivités sur alpha KGDHC Anticorps
Humain, Souris, Rat
Hôte
Toutes les hôtes sur alpha KGDHC Anticorps
Lapin
Clonalité
Toutes les clonalités sur alpha KGDHC Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers alpha KGDHC Anticorps
Cet anticorp alpha KGDHC est non-conjugé
Application
Tous les applications à travers alpha KGDHC Anticorps.
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
Purification
Affinity purification
Immunogène
Recombinant protein of human OGDH
Isotype
IgG
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Alternatives
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Information d'application
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Indications d'application
WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200
Restrictions
For Research Use only
Stockage
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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 -20C. Avoid freeze / thaw cycles.
Détails sur alpha KGDHC
(cache)
Antigène
alpha KGDHC (alphaKGDHC)
(alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
Autre désignation
OGDH (alphaKGDHC Produits )
Synonymes
anticorps AKGDH, anticorps E1k, anticorps OGDC, anticorps 2210403E04Rik, anticorps 2210412K19Rik, anticorps AA409584, anticorps d1401, anticorps mKIAA4192, anticorps oxoglutarate dehydrogenase, anticorps oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide), anticorps OGDH, anticorps 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
115.935 kDa
ID gène
4967
UniProt
Q02218
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