The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 alpha 1 subunit containing the E1 active site, and plays a key role in the function of the PDH complex. Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Stoccaggio: This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.
Isotipo: IgG
Clonalità: Monoclonal
Clone: 6B2
Coniugazione: Unconjugated
Applicazione: ICC/IF
Diluizione: ICC/IF 1:20-1:100
Simbolo target: PDHA1
Ig target: PDHA1;PDHA;PDHAD;PDHCE1A;PHE1A;E1 alpha polypeptide 1;mitochondrial;ODPA;PDH;PDHE1 A type I;PDHE1-A type I;PDHα;Pyruvate Dehydrogenase (lipoamide) alpha 1;Pyruvate dehydrogenase complex;Pyruvate Dehydrogenase E1 alpha;Pyruvate dehydrogenase E1 component subunit alpha;somatic form
Area di ricerca:Signal Transduction;Cancer;Metabolism
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