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丙酮酸脱氢酶复合体成分X(PDHX)抗体
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。

丙酮酸脱氢酶复合物X蛋白抗体
Anti-PDHX
靶标:

PDHX


产品别名:

DLDBP; E3BP; OPDX; PDHXD; PDX1; proX; PDHX; pyruvate dehydrogenase complex component X; pyruvate dehydrogenase complex component X; pyruvate dehydrogenase protein X component, mitochondrial; dihydrolipoamide dehydrogenase-binding protein of pyruvate dehydrogenase complex; lipoyl-containing pyruvate dehydrogenase complex component X; pyruvate dehydrogenase complex, E3-binding protein subunit; pyruvate dehydrogenase complex, lipoyl-containing component X; 丙酮酸脱氢酶复合体成分X(PDHX); 丙酮酸脱氢酶复合物X蛋白;


背景信息:
The pyruvate dehydrogenase (PDH) complex is located in the mitochondrial matrix and catalyzes the conversion of pyruvate to acetyl coenzyme A. The PDH complex thereby links glycolysis to Krebs cycle. The PDH complex contains three catalytic subunits, E1, E2, and E3, two regulatory subunits, E1 kinase and E1 phosphatase, and a non-catalytic subunit, E3 binding protein (E3BP). This gene encodes the E3 binding protein subunit; also known as component X of the pyruvate dehydrogenase complex. This protein tethers E3 dimers to the E2 core of the PDH complex. Defects in this gene are a cause of pyruvate dehydrogenase deficiency which results in neurological dysfunction and lactic acidosis in infancy and early childhood. This protein is also a minor antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC eventually leads to cirrhosis and liver failure. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009],
 
 
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