Anti-PDHX antibody

Polyclonal

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

O00330

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.

PDHX

Rabbit polyclonal against PDHX

Calculated: 29kDa/51kDa/54kDa. Observed: 54kDa

Anti-Pyruvate Dehydrogenase Protein X Component-Mitochondrial antibody
Anti-Dihydrolipoamide Dehydrogenase-Binding Protein Of Pyruvate Dehydrogenase Complex antibody
Anti-E3-Binding Protein antibody
Anti-E3bp antibody
Anti-Lipoyl-Containing Pyruvate Dehydrogenase Complex Component X antibody
Anti-Prox antibody
Anti-PDHX PDX1 antibody

FOR RESEARCH USE ONLY (RUO).