BDHA1 Antibody (Center) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | P08559 |
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Other Accession | NP_000275.1 |
Clone Names | 90713270 |
Gene ID | 5160 |
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Other Names | Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial, PDHE1-A type I, PDHA1, PHE1A |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | PDHA1 |
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Synonyms | PHE1A |
Function | The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby links the glycolytic pathway to the tricarboxylic cycle. |
Cellular Location | Mitochondrion matrix. |
Tissue Location | Ubiquitous. |
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Provided below are standard protocols that you may find useful for product applications.
Background
The pyruvate dehydrogenase (PDH) complex is anuclear-encoded mitochondrial multienzyme complex that catalyzesthe overall conversion of pyruvate to acetyl-CoA and CO(2), andprovides the primary link between glycolysis and the tricarboxylicacid (TCA) cycle. The PDH complex is composed of multiple copies ofthree enzymatic components: pyruvate dehydrogenase (E1),dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase(E3). The E1 enzyme is a heterotetramer of two alpha and two betasubunits. This gene encodes the E1 alpha 1 subunit containing theE1 active site, and plays a key role in the function of the PDHcomplex.
References
Glushakova, L.G., et al. Mol. Genet. Metab. 98(3):289-299(2009)Joao Silva, M., et al. Eur. J. Pediatr. 168(1):17-22(2009)Boichard, A., et al. Mol. Genet. Metab. 93(3):323-330(2008)
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