Pyruvate dehydrogenase (PDH) subunit E1 alpha monoclonal antibody

Catalog No. MSP07

$325.00 - 100 µg


This antibody can also be purchased as part of a Sample Pack.

UniProt Number: P08559
Alternate Names: Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial, PDHE1-A type I
Structure and Function: The pyruvate dehydrogenase complex contains three different subunits including the pyruvate dehydrogenase E1 subunit.The PDH complex is responsible for catalyzing the formation of acetyl-CoA and CO2 from pyruvate.
Disease Associations: Enzyme deficiency of the PDH E1 subunit of the PDH complex commonly results in lactic acidosis. There are a wide range of symptoms that characterize this disorder including neonatal death, developmental delay, seizures, ataxia, apnea and X-link Leigh Syndrome (LS). This syndrome presents itself with necrotic lesions that are located symmetrically in both sides the subcortical brain.



 
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Product Specifications
 
Applications: Western blotting and Immunocytochemistry (heat-induced antigen-retrieval improves signal)
Species Reactivity: human, bovine, mouse, rat, Drosophila melanogaster and C. elegans
Host Species: mouse
Isotype: IgG1, k
Clone ID: 8D10E6
Concentration: 1.0 mg/mL in Hepes-Buffered Saline (HBS) with 0.02% azide as a preservative.
Suggested Working Concentration: 0.5-1.0 µg/mL for Western blotting
1 µg/mL for Immunocytochemistry
Storage Conditions: 4°C
Country of Origin: USA


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Figure 1. Isolated mitochondria from human heart (lane 1), bovine heart (lane 2), rat heart (lane 3), mouse heart (lane 4), and HepG2 (lane 5) detected with (MSP07) anti-subunit E1 alpha antibody.
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Figure 2. Mitochondrial localization of PDH in cultured, normal human fibroblasts labeled with anti-PDH-E1 alpha mAb 8D10E6 (MSP07) as the primary antibody and an Alexa Fluor® 488 goat anti-mouse secondary antibody.


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Downloadable Documents


   Technical Data Sheet

   Western blotting Protocol

   Immunocytochemistry Protocol

   PDH Playbook


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Published Studies Using This Product: Glushakova et al., 2009. AAV3-mediated transfer and expression of the pyruvate dehydrogenase E1 alpha subunit gene causes metabolic remodeling and apoptosis of human liver cancer cells.

Cox et al., 2009. Clueless, a conserved Drosophila gene required for mitochondrial subcellular localization, interacts genetically with parkin.

Stenson et al., 2009. Activation of liver X receptor regulates substrate oxidation in white adipocytes.

Ostergaard et al., 2009. Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency.

Greiss et al., 2008. C. elegans SIR-2.1 translocation is linked to a proapoptotic pathway parallel to cep-1/p53 during DNA damage-induced apoptosis.


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