Anti-ATP5A antibody [15H4C4] - Mitochondrial Marker (ab14748)

ab14748 has been referenced in 27 publications.

• Gorai T  et al. F1Fo-ATPase, F-type proton-translocating ATPase, at the plasma membrane is critical for efficient influenza virus budding. Proc Natl Acad Sci U S A 109:4615-20 (2012). PubMed: 22393008
• Ferreira M  et al. Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1. Neurogenetics 12:9-17 (2011). PubMed: 21203893
• Celotto AM  et al. Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction. PLoS One 6:e25823 (2011). WB ; Fruit fly (Drosophila melanogaster) . PubMed: 21991365
• Nadanaciva S  et al. High-content screening for compounds that affect mtDNA-encoded protein levels in eukaryotic cells. J Biomol Screen 15:937-48 (2010). PubMed: 20625181
• Khanna MR  et al. Towards a membrane proteome in Drosophila: a method for the isolation of plasma membrane. BMC Genomics 11:302 (2010). PubMed: 20462449
• Escobar-Alvarez S  et al. Inhibition of human peptide deformylase disrupts mitochondrial function. Mol Cell Biol 30:5099-109 (2010). WB ; Human . PubMed: 20805355
• Brys K  et al. Disruption of insulin signalling preserves bioenergetic competence of mitochondria in ageing Caenorhabditis elegans. BMC Biol 8:91 (2010). WB ; Caenorhabditis elegans . PubMed: 20584279
• Ziviani E  et al. Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin. Proc Natl Acad Sci U S A 107:5018-23 (2010). WB ; Fruit fly (Drosophila melanogaster) . PubMed: 20194754
• Cox RT & Spradling AC Clueless, a conserved Drosophila gene required for mitochondrial subcellular localization, interacts genetically with parkin. Dis Model Mech 2:490-9 (2009). PubMed: 19638420
• Yang JY  et al. Insulin stimulates Akt translocation to mitochondria: implications on dysregulation of mitochondrial oxidative phosphorylation in diabetic myocardium. J Mol Cell Cardiol 46:919-26 (2009). PubMed: 19249309
• Liu K  et al. Functional analysis of FSP27 protein regions for lipid droplet localization, caspase-dependent apoptosis, and dimerization with CIDEA. Am J Physiol Endocrinol Metab 297:E1395-413 (2009). WB ; African Green Monkey . PubMed: 19843876
• Wang N  et al. Comparative proteome profile of immature rat ovary during primordial follicle assembly and development. Proteomics 9:3425-34 (2009). PubMed: 19557761
• Greiss S  et al. C. elegans SIR-2.1 translocation is linked to a proapoptotic pathway parallel to cep-1/p53 during DNA damage-induced apoptosis. Genes Dev 22:2831-42 (2008). PubMed: 18923081
• Khidr L  et al. Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells. J Biol Chem 283:27064-73 (2008). PubMed: 18678873
• Mast JD  et al. Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy. Development 135:2669-79 (2008). PubMed: 18599508
• Yang J  et al. C-reactive protein augments hypoxia-induced apoptosis through mitochondrion-dependent pathway in cardiac myocytes. Mol Cell Biochem 310:215-26 (2008). PubMed: 18165866
• Kim M  et al. Increased expression of the F(1)F(o) ATP synthase in response to iron in heart mitochondria. BMB Rep 41:153-7 (2008). PubMed: 18315952
• Watanabe Y  et al. Adherent monomer-misfolded SOD1. PLoS One 3:e3497 (2008). PubMed: 18946506
• Rea SL  et al. Relationship between mitochondrial electron transport chain dysfunction, development, and life extension in Caenorhabditis elegans. PLoS Biol 5:e259 (2007). PubMed: 17914900
• Li Y  et al. An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria. J Biol Chem 282:17557-62 (2007). PubMed: 17452320
• Park JS  et al. Yeast NDI1 improves oxidative phosphorylation capacity and increases protection against oxidative stress and cell death in cells carrying a Leber's hereditary optic neuropathy mutation. Biochim Biophys Acta 1772:533-42 (2007). PubMed: 17320357
• Ventura N & Rea SL Caenorhabditis elegans mitochondrial mutants as an investigative tool to study human neurodegenerative diseases associated with mitochondrial dysfunction. Biotechnol J 2:584-95 (2007). PubMed: 17443764
• Cortés-Hernández P  et al. ATP6 homoplasmic mutations inhibit and destabilize the human F1F0-ATP synthase without preventing enzyme assembly and oligomerization. J Biol Chem 282:1051-8 (2007). PubMed: 17121862
• Stiburek L  et al. Knockdown of human Oxa1l impairs the biogenesis of F1Fo-ATP synthase and NADH:ubiquinone oxidoreductase. J Mol Biol 374:506-16 (2007). PubMed: 17936786
• McQuibban GA  et al. Normal mitochondrial dynamics requires rhomboid-7 and affects Drosophila lifespan and neuronal function. Curr Biol 16:982-9 (2006). PubMed: 16713954
• Wall JA  et al. Alterations in oxidative phosphorylation complex proteins in the hearts of transgenic mice that overexpress the p38 MAP kinase activator, MAP kinase kinase 6. Am J Physiol Heart Circ Physiol 291:H2462-72 (2006). WB ; Human, Mouse . PubMed: 16766635
• Capaldi RA  et al. Immunological approaches to the characterization and diagnosis of mitochondrial disease. Mitochondrion 4:417-26 (2004). PubMed: 16120403