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alpha KGDHC antibody
alphaKGDHC
Reactivity: Human, Rat, Mouse
WB, IHC, ELISA, IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-alpha KGDHC Antibody
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Target
See all alpha KGDHC (alphaKGDHC) Antibodies
alpha KGDHC (alphaKGDHC)
(alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
Reactivity
All reactivities for alpha KGDHC antibodies
Human, Rat, Mouse
Host
All hosts for alpha KGDHC antibodies
Rabbit
Clonality
All clonalities for alpha KGDHC antibodies
Polyclonal
Conjugate
All conjugates for alpha KGDHC antibodies
This alpha KGDHC antibody is un-conjugated
Application
All applications for alpha KGDHC antibodies
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
Purification
Immunogen affinity purified
Purity
≥95 % as determined by SDS-PAGE
Immunogen
oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)
Isotype
IgG
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Discover our top product alphaKGDHC Primary Antibody
Alternatives
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Application Details
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Application Notes
WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Expiry Date
12 months
Target Details for alpha KGDHC
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Target
alpha KGDHC (alphaKGDHC)
(alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
Alternative Name
OGDH (alphaKGDHC Products )
Synonyms
AKGDH antibody, E1k antibody, OGDC antibody, 2210403E04Rik antibody, 2210412K19Rik antibody, AA409584 antibody, d1401 antibody, mKIAA4192 antibody, oxoglutarate dehydrogenase antibody, oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) antibody, OGDH antibody, Ogdh antibody
Background
Synonyms:AKGDH Background: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.
Molecular Weight
116 kDa
Gene ID
4967
UniProt
Q02218
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