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8ODP Polyclonal Antibody |
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JOT-AP08520-100ul | Jotbody | 100ul | 220 EUR |
8ODP Polyclonal Antibody |
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JOT-AP08520-50ul | Jotbody | 50ul | 144 EUR |
8ODP Polyclonal Antibody |
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MBS8529721-01mg | MyBiosource | 0.1mg | 305 EUR |
8ODP Polyclonal Antibody |
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MBS8529721-01mLAF405L | MyBiosource | 0.1mL(AF405L) | 465 EUR |
8ODP Polyclonal Antibody |
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MBS8529721-01mLAF405S | MyBiosource | 0.1mL(AF405S) | 465 EUR |
8ODP Polyclonal Antibody |
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MBS8529721-01mLAF610 | MyBiosource | 0.1mL(AF610) | 465 EUR |
8ODP Polyclonal Antibody |
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MBS8529721-01mLAF635 | MyBiosource | 0.1mL(AF635) | 465 EUR |
8ODP Polyclonal Antibody |
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UB-GEN-5123 | UpingBio | 100 ul | 200 EUR |
ODPX Rabbit Polyclonal Antibody |
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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. |
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ODPX Rabbit Polyclonal Antibody |
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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. |
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ODPX Rabbit Polyclonal Antibody |
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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. |
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ODPA Rabbit Polyclonal Antibody |
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ES9008-100ul | ELK Biotech | 100ul | 124 EUR |
Description: WB, ELISA |
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ODPA Rabbit Polyclonal Antibody |
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ES9008-50ul | ELK Biotech | 50ul | 74 EUR |
Description: WB, ELISA |
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ODPB Rabbit Polyclonal Antibody |
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ES10077-100ul | ELK Biotech | 100ul | 124 EUR |
Description: WB, ELISA |
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ODPB Rabbit Polyclonal Antibody |
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ES10077-50ul | ELK Biotech | 50ul | 74 EUR |
Description: WB, ELISA |
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ODPX Rabbit Polyclonal Antibody |
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JOT-AP11651-100ul | Jotbody | 100ul | 220 EUR |
ODPX Rabbit Polyclonal Antibody |
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JOT-AP11651-50ul | Jotbody | 50ul | 144 EUR |
8ODP Antibody |
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C42406-100ul | Assay Biotech | 100μl | 217 EUR |
Description: 8ODP Rabbit Polyclonal Antibody |