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A12477

OGDH Rabbit polyclonal antibody

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£152.00

SKU:
A12477
Additional Names:
AKGDH|E1k|E1o|KGD1|OGDC|OGDH|OGDH-E1|OGDH2|OGDHD
Application:
ELISA, WB, IHC-P, IF, ICC
Molecular Weight:
116kDa
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Abclonal
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulation:
Unmodified
Sequence:
DPLGILDADLDSSVPADIISSTDKLGFYGLDESDLDKVFHLPTTTFIGGQESALPLREIIRRLEMAYCQHIGVEFMFINDLEQCQWIRQKFETPGIMQFTNEEKRTLLARLVRSTRFEEFLQRKWSSEKRFGLEGCEVLIPALKTIIDKSSENGVDYVIMGMPHRGRLNVLANVIRKELEQIFCQFDSKLEAADEGSGDVKYHLGMYHRRINRVTDRNITLSLVANPSHLEAADPVVMGKTKAEQFYCGDTEGKKVRPRERRARQIVKAPCSSMEFRSPT
Uniprot:
Q02218
Synonyms:
2-oxoglutarate dehydrogenase complex component E1;2-oxoglutarate dehydrogenase, mitochondrial;AKGDH;Alpha-ketoglutarate dehydrogenase;E1k;KGD1;OGDC;OGDC-E1;OGDH2;oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide);oxoglutarate decarboxylase;oxoglutarate dehydrogenase (succinyl-transferring);testicular tissue protein Li 131
Extra Details:
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.
Shipping Conditions:
Blue Ice