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alphaKGDHC encodes one subunit of the 2-oxoglutarate dehydrogenase complex. Additionally we are shipping alpha Ketoglutarate Dehydrogenase Kits (21) and alpha Ketoglutarate Dehydrogenase Proteins (5) and many more products for this protein.
Showing 10 out of 51 products:
Human Polyclonal alphaKGDHC Primary Antibody for IHC (p), WB - ABIN657365
Habelhah, Laine, Erdjument-Bromage, Tempst, Gershwin, Bowtell, Ronai: Regulation of 2-oxoglutarate (alpha-ketoglutarate) dehydrogenase stability by the RING finger ubiquitin ligase Siah. in The Journal of biological chemistry 2004
Show all 2 references for ABIN657365
Chicken Polyclonal alphaKGDHC Primary Antibody for WB - ABIN2787780
van Bever, Balemans, Duval, Jespers, Eyskens, van Hul, Courtens: Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome. in American journal of medical genetics. Part A 2007
Acute inhibition of alpha-ketoglutarate dehydrogenase produces effects on calcium opposite to those in Alzheimer's disease (AD), while the chronic or long-term inhibition of alpha-KGDHC mimicked the AD-related changes in calcium.
2-oxoglutarate (alpha-ketoglutarate) dehydrogenase stability is regulated by the RING finger ubiquitin ligase Siah
Reduction in the E2k (show DLST Antibodies) subunit of the alpha-ketoglutarate dehydrogenase complex has effects independent of complex activity.
The nitration degree of alpha-OGDH for diabetic mouse is higher than that for control mouse, indicating that alpha-OGDH of the diabetic mouse suffered from more intense oxidative damage.
Alpha-ketoglutarate dehydrogenase is a primary site of ROS (show ROS1 Antibodies) production in normally functioning mitochondria.
In the postnatal mouse brain,high mRNA levels of d1401/Ogdh were observed in the olfactory bulb, hippocampus, cerebellum, and pons.
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.
2-oxoglutarate dehydrogenase, mitochondrial
, 2-oxoglutarate dehydrogenase complex component E1
, oxoglutarate decarboxylase
, oxoglutarate dehydrogenase (succinyl-transferring)
, 2-oxoglutarate dehydrogenase E1 component, mitochondrial
, alpha-ketoglutarate dehydrogenase
, oxoglutarate dehydrogenase (lipoamide)