{"product_id":"cst-15289s","title":"CST,  15289S, Phospho-Pyruvate Dehydrogenase alpha1 (Ser232) Antibody","description":"Polyclonal Antibody for studying PDHA1 (Ser232) phosphate. Validated for Western Blotting. Highly specific and rigorously validated in-house, Phospho-Pyruvate Dehydrogenase alpha1 (Ser232) Antibody (CST #15289) is ready to ship.\n\n\u003cb\u003eProduct Usage Information\u003c\/b\u003e\nWestern Blotting: 1:1000\n\u003cb\u003eStorage\u003c\/b\u003e\nSupplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg\/mL BSA, and 50% glycerol. Store at -20°C. Do not aliquot the antibody.\n\u003cb\u003eProtocol\u003c\/b\u003e\nAvailable protocols: Western Blotting\n\u003cb\u003eSpecificity \/ Sensitivity\u003c\/b\u003e\nPhospho-Pyruvate Dehydrogenase alpha1 (Ser232) Antibody recognizes endogenous levels of pyruvate dehydrogenase Î±1 protein only when phosphorylated at Ser232.\nSpecies Reactivity: Human\n\u003cb\u003eSource \/ Purification\u003c\/b\u003e\nPolyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Ser232 of human pyruvate dehydrogenase Î±1 protein. Antibodies are purified by peptide affinity chromatography.\n\u003cb\u003eBackground\u003c\/b\u003e\nThe pyruvate dehydrogenase complex catalyzes the conversion of pyruvate and CoA into acetyl-CoA and CO in the presence of NAD . Acetyl-CoA then goes into the citric acid cycle where it reacts with oxaloacetate to form citrate. The reaction of oxidative decarboxylation of pyruvate serves as a critical link between glycolysis and the citric acid cycle. In mammalian cells, the pyruvate dehydrogenase complex is located in the mitochondrial matrix (1). This complex is composed of three enzymes: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2), and dihydrolipoamide dehydrogenase (E3). Pyruvate dehydrogenase (E1) consists of two subunits: Î± and Î². This enzyme catalyzes the removal of CO from pyruvate. Mutations in the Î± subunits of pyruvate dehydrogenase (E1) lead to congenital defects that are usually associated with lactic acidosis, neurodegeneration, and early death (2). Pyruvate dehydrogenase kinase 1 phosphorylates pyruvate dehydrogenase (E1) Î±1 subunit at Ser232 and Ser300, which is important for ubiquitin-dependent degradation of this subunit (3).\n\u003cb\u003eAlternate Names\u003c\/b\u003e\nODPA; PDHA; PDHA1; PDHAD; PDHCE1A; PDHE1-A type I; PHE1A; pyruvate dehydrogenase (lipoamide) alpha 1; pyruvate dehydrogenase alpha 1; pyruvate dehydrogenase complex, E1-alpha polypeptide 1; pyruvate dehydrogenase E1 alpha 1; pyruvate dehydrogenase E1 alpha 1 subunit; Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial; pyruvate dehydrogenase E1 subunit alpha 1\n\n\u003cb\u003eSpecification\u003c\/b\u003e\n\nREACTIVITY: H\nSENSITIVITY: Endogenous\nMW (kDa): 43\nSOURCE: Rabbit","brand":"CST","offers":[{"title":"Default Title","offer_id":46797625524393,"sku":"15289S","price":0.99,"currency_code":"USD","in_stock":true}],"url":"https:\/\/iright.com\/products\/cst-15289s","provider":"Iright","version":"1.0","type":"link"}