8ODP Rabbit Polyclonal Antibody

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8ODP Polyclonal Antibody

JOT-AP08520-100ul Jotbody 100ul 220 EUR

8ODP Polyclonal Antibody

JOT-AP08520-50ul Jotbody 50ul 144 EUR

8ODP Polyclonal Antibody

MBS8529721-01mg MyBiosource 0.1mg 305 EUR

8ODP Polyclonal Antibody

MBS8529721-01mLAF405L MyBiosource 0.1mL(AF405L) 465 EUR

8ODP Polyclonal Antibody

MBS8529721-01mLAF405S MyBiosource 0.1mL(AF405S) 465 EUR

8ODP Polyclonal Antibody

MBS8529721-01mLAF610 MyBiosource 0.1mL(AF610) 465 EUR

8ODP Polyclonal Antibody

MBS8529721-01mLAF635 MyBiosource 0.1mL(AF635) 465 EUR

8ODP Polyclonal Antibody

UB-GEN-5123 UpingBio 100 ul 200 EUR

ODPX Rabbit Polyclonal Antibody

BT-AP11651-100ul Jiaxing Korain Biotech Ltd (BT Labs) 100ul Ask for price
Description: 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.

ODPX Rabbit Polyclonal Antibody

BT-AP11651-20ul Jiaxing Korain Biotech Ltd (BT Labs) 20ul Ask for price
Description: 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.

ODPX Rabbit Polyclonal Antibody

BT-AP11651-50ul Jiaxing Korain Biotech Ltd (BT Labs) 50ul Ask for price
Description: 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.

ODPA Rabbit Polyclonal Antibody

ES9008-100ul ELK Biotech 100ul 124 EUR
Description: WB, ELISA

ODPA Rabbit Polyclonal Antibody

ES9008-50ul ELK Biotech 50ul 74 EUR
Description: WB, ELISA

ODPB Rabbit Polyclonal Antibody

ES10077-100ul ELK Biotech 100ul 124 EUR
Description: WB, ELISA

ODPB Rabbit Polyclonal Antibody

ES10077-50ul ELK Biotech 50ul 74 EUR
Description: WB, ELISA

ODPX Rabbit Polyclonal Antibody

JOT-AP11651-100ul Jotbody 100ul 220 EUR

ODPX Rabbit Polyclonal Antibody

JOT-AP11651-50ul Jotbody 50ul 144 EUR

8ODP Antibody

C42406-100ul Assay Biotech 100μl 217 EUR
Description: 8ODP Rabbit Polyclonal Antibody