Anti-NDUFA9 antibody [20C11B11B11] (ab14713)

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ab14713 has been referenced in 83 publications.

  • Sakakibara I  et al. Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle. Skelet Muscle 6:30 (2016). WB ; Mouse . PubMed: 27597886
  • Pérez-Pérez R  et al. COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation. Cell Rep 16:2387-98 (2016). WB . PubMed: 27545886
  • Doerrier C  et al. Identification of mitochondrial deficits and melatonin targets in liver of septic mice by high-resolution respirometry. Life Sci 121:158-65 (2015). PubMed: 25498899
  • Davoudi M  et al. Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency. PLoS One 9:e86767 (2014). WB ; Mouse . PubMed: 24466228
  • Bourens M  et al. Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase. Hum Mol Genet N/A:N/A (2014). Human . PubMed: 24403053
  • Jannig PR  et al. Autophagy signaling in skeletal muscle of infarcted rats. PLoS One 9:e85820 (2014). WB ; Rat . PubMed: 24427319
  • Hornig-Do HT  et al. Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations. EMBO Mol Med 6:183-93 (2014). WB ; Human . PubMed: 24413189
  • Metodiev MD  et al. NSUN4 is a dual function mitochondrial protein required for both methylation of 12S rRNA and coordination of mitoribosomal assembly. PLoS Genet 10:e1004110 (2014). WB ; Mouse . PubMed: 24516400
  • Guarani V  et al. TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex. Mol Cell Biol 34:847-61 (2014). PubMed: 24344204
  • Miwa S  et al. Low abundance of the matrix arm of complex I in mitochondria predicts longevity in mice. Nat Commun 5:3837 (2014). WB ; Mouse . PubMed: 24815183
  • Huang R  et al. Megakaryocytic Differentiation of K562 Cells Induced by PMA Reduced the Activity of Respiratory Chain Complex IV. PLoS One 9:e96246 (2014). PubMed: 24817082
  • Yarham JW  et al. Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA. PLoS Genet 10:e1004424 (2014). WB ; Human . PubMed: 24901367
  • Porter GA  et al. SIRT3 deficiency exacerbates ischemia-reperfusion injury: implication for aged hearts. Am J Physiol Heart Circ Physiol 306:H1602-9 (2014). PubMed: 24748594
  • Wilson WC  et al. A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression. Hum Mol Genet N/A:N/A (2014). WB ; Human . PubMed: 25008111
  • Zurita Rendón O  et al. The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesis. Hum Mol Genet 23:5159-70 (2014). Mouse . PubMed: 24838397
  • Invernizzi F  et al. Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations. Front Genet 5:412 (2014). PubMed: 25477904
  • Beutner G  et al. Initiation of electron transport chain activity in the embryonic heart coincides with the activation of mitochondrial complex 1 and the formation of supercomplexes. PLoS One 9:e113330 (2014). WB ; Mouse . PubMed: 25427064
  • Kumarasamy S  et al. Construction of two novel reciprocal conplastic rat strains and characterization of cardiac mitochondria. Am J Physiol Heart Circ Physiol 304:H22-32 (2013). WB ; Rat . PubMed: 23125210
  • Chung DJ  et al. Changes in the mitochondrial phosphoproteome during mammalian hibernation. Physiol Genomics 45:389-99 (2013). WB . PubMed: 23572536
  • Jonckheere AI  et al. A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy. Brain 136:1544-54 (2013). PubMed: 23599390
  • Pitceathly RD  et al. NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease. Cell Rep 3:1795-805 (2013). WB . PubMed: 23746447
  • Palin EJ  et al. Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders. Brain 136:2379-92 (2013). Human . PubMed: 23811324
  • Ghelli A  et al. The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes. Hum Mol Genet 22:2141-51 (2013). PubMed: 23418307
  • Bartoletti-Stella A  et al. Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1a. Cell Death Dis 4:e663 (2013). WB ; Human . PubMed: 23764844
  • Tanaka A  et al. The overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in mice. PLoS One 8:e67642 (2013). WB ; Mouse . PubMed: 23840758
  • Kovárová N  et al. High molecular weight forms of mammalian respiratory chain complex II. PLoS One 8:e71869 (2013). WB ; Human . PubMed: 23967256
  • Domenighetti AA  et al. Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice. Hum Mol Genet N/A:N/A (2013). Mouse . PubMed: 23975679
  • Hämäläinen RH  et al. Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model. Proc Natl Acad Sci U S A 110:E3622-30 (2013). PubMed: 24003133
  • Almalki A  et al. Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. Biochim Biophys Acta 1842:56-64 (2013). Human . PubMed: 24161539
  • Schlehe JS  et al. The mitochondrial disease associated protein Ndufaf2 is dispensable for Complex-1 assembly but critical for the regulation of oxidative stress. Neurobiol Dis 58:57-67 (2013). Human . PubMed: 23702311
  • Yatsuga S & Suomalainen A Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice. Hum Mol Genet 21:526-35 (2012). PubMed: 22012983
  • Houstek J  et al. Nonsynonymous variants in mt-Nd2, mt-Nd4, and mt-Nd5 are linked to effects on oxidative phosphorylation and insulin sensitivity in rat conplastic strains. Physiol Genomics 44:487-94 (2012). WB ; Rat . PubMed: 22414913
  • Stiburek L  et al. YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation. Mol Biol Cell 23:1010-23 (2012). PubMed: 22262461
  • Danhauser K  et al. Cellular rescue-assay aids verification of causative DNA-variants in mitochondrial complex I deficiency. Mol Genet Metab 103:161-6 (2011). WB ; Human . PubMed: 21458341
  • 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
  • Strub GM  et al. Sphingosine-1-phosphate produced by sphingosine kinase 2 in mitochondria interacts with prohibitin 2 to regulate complex IV assembly and respiration. FASEB J 25:600-12 (2011). PubMed: 20959514
  • Thomas RR  et al. Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin. Mitochondrion 11:108-18 (2011). PubMed: 20727424
  • Dennerlein S  et al. Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit. Biochem J 430:551-8 (2010). PubMed: 20604745
  • Berger Z  et al. Membrane localization of LRRK2 is associated with increased formation of the highly active LRRK2 dimer and changes in its phosphorylation. Biochemistry 49:5511-23 (2010). PubMed: 20515039
  • Ylikallio E  et al. High mitochondrial DNA copy number has detrimental effects in mice. Hum Mol Genet 19:2695-705 (2010). PubMed: 20413656
  • Wydro M  et al. Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibition. Nucleic Acids Res 38:3732-42 (2010). PubMed: 20144953
  • Baracca A  et al. Mitochondrial Complex I decrease is responsible for bioenergetic dysfunction in K-ras transformed cells. Biochim Biophys Acta 1797:314-23 (2010). PubMed: 19931505
  • Kachadourian R  et al. Casiopeína IIgly-induced oxidative stress and mitochondrial dysfunction in human lung cancer A549 and H157 cells. Toxicology 268:176-83 (2010). PubMed: 20026372
  • Gegg ME  et al. Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy. Hum Mol Genet 19:4861-70 (2010). PubMed: 20871098
  • Fassone E  et al. FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. Hum Mol Genet 19:4837-47 (2010). PubMed: 20858599
  • Gerards M  et al. Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome. J Med Genet 47:507-12 (2010). PubMed: 19542079
  • Lynn EG  et al. Transient upregulation of PGC-1alpha diminishes cardiac ischemia tolerance via upregulation of ANT1. J Mol Cell Cardiol 49:693-8 (2010). WB ; Rat . PubMed: 20600099
  • Tuppen HA  et al. The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. Brain 133:2952-63 (2010). WB ; Human . PubMed: 20819849
  • Ahola-Erkkilä S  et al. Ketogenic diet slows down mitochondrial myopathy progression in mice. Hum Mol Genet 19:1974-84 (2010). WB ; Mouse . PubMed: 20167576
  • Iyer S  et al. Recombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression. Mitochondrion 9:196-203 (2009). PubMed: 19460293
  • Galati D  et al. Role of nuclear-encoded subunit Vb in the assembly and stability of cytochrome c oxidase complex: implications in mitochondrial dysfunction and ROS production. Biochem J 420:439-49 (2009). PubMed: 19338496
  • Palmfeldt J  et al. Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress. Proteome Sci 7:20 (2009). PubMed: 19476632
  • Vempati UD  et al. Lack of cytochrome c in mouse fibroblasts disrupts assembly/stability of respiratory complexes I and IV. J Biol Chem 284:4383-91 (2009). PubMed: 19075019
  • Hu Y  et al. Increased enzymatic O-GlcNAcylation of mitochondrial proteins impairs mitochondrial function in cardiac myocytes exposed to high glucose. J Biol Chem 284:547-55 (2009). PubMed: 19004814
  • Missihoun C  et al. Myocardial oxidative stress, osteogenic phenotype, and energy metabolism are differentially involved in the initiation and early progression of delta-sarcoglycan-null cardiomyopathy. Mol Cell Biochem 321:45-52 (2009). PubMed: 18726675
  • Area-Gomez E  et al. Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria. Am J Pathol 175:1810-6 (2009). PubMed: 19834068
  • Gómez LA  et al. Supercomplexes of the mitochondrial electron transport chain decline in the aging rat heart. Arch Biochem Biophys 490:30-5 (2009). PubMed: 19679098
  • Arthur CR  et al. Parkinson's disease brain mitochondria have impaired respirasome assembly, age-related increases in distribution of oxidative damage to mtDNA and no differences in heteroplasmic mtDNA mutation abundance. Mol Neurodegener 4:37 (2009). PubMed: 19775436
  • Rackham O  et al. Pentatricopeptide repeat domain protein 1 lowers the levels of mitochondrial leucine tRNAs in cells. Nucleic Acids Res 37:5859-67 (2009). PubMed: 19651879
  • Grünewald A  et al. Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology. Exp Neurol 219:266-73 (2009). PubMed: 19500570
  • Sheftel AD  et al. Human ind1, an iron-sulfur cluster assembly factor for respiratory complex I. Mol Cell Biol 29:6059-73 (2009). WB ; Human . PubMed: 19752196
  • Keeney PM  et al. Mitochondrial gene therapy augments mitochondrial physiology in a Parkinson's disease cell model. Hum Gene Ther 20:897-907 (2009). WB ; Human . PubMed: 19374590
  • Hakonen AH  et al. Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. Hum Mol Genet 17:3822-35 (2008). PubMed: 18775955
  • Calvaruso MA  et al. Electrophoresis techniques to investigate defects in oxidative phosphorylation. Methods 46:281-7 (2008). PubMed: 18948205
  • Cooper MP  et al. Modulation of PGC-1 coactivator pathways in brown fat differentiation through LRP130. J Biol Chem 283:31960-7 (2008). PubMed: 18728005
  • Minai L  et al. Mitochondrial respiratory chain complex assembly and function during human fetal development. Mol Genet Metab 94:120-6 (2008). PubMed: 18249146
  • Son M  et al. Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein. J Biol Chem 283:12267-75 (2008). PubMed: 18334481
  • Fornuskova D  et al. The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues. Biochim Biophys Acta 1782:317-25 (2008). PubMed: 18319067
  • Mayr JA  et al. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clin Cancer Res 14:2270-5 (2008). PubMed: 18413815
  • Lebon S  et al. A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome. Mol Genet Metab 92:104-8 (2007). PubMed: 17604671
  • Pravenec M  et al. Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains. Genome Res 17:1319-26 (2007). PubMed: 17693571
  • 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
  • Cheung EC  et al. Dissociating the dual roles of apoptosis-inducing factor in maintaining mitochondrial structure and apoptosis. EMBO J 25:4061-73 (2006). PubMed: 16917506
  • Pye D  et al. Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants. Nucleic Acids Res 34:e95 (2006). PubMed: 16885236
  • Wang Y & Bogenhagen DF Human mitochondrial DNA nucleoids are linked to protein folding machinery and metabolic enzymes at the mitochondrial inner membrane. J Biol Chem 281:25791-802 (2006). PubMed: 16825194
  • Gybina AA & Prohaska JR Variable response of selected cuproproteins in rat choroid plexus and cerebellum following perinatal copper deficiency. Genes Nutr 1:51-9 (2006). PubMed: 18850220
  • Leshinsky-Silver E  et al. Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene. Biochem Biophys Res Commun 334:582-7 (2005). PubMed: 16023078
  • Schilling B  et al. Rapid purification and mass spectrometric characterization of mitochondrial NADH dehydrogenase (Complex I) from rodent brain and a dopaminergic neuronal cell line. Mol Cell Proteomics 4:84-96 (2005). PubMed: 15591592
  • Ramachandran A  et al. Chronic exposure to nitric oxide alters the free iron pool in endothelial cells: role of mitochondrial respiratory complexes and heat shock proteins. Proc Natl Acad Sci U S A 101:384-9 (2004). PubMed: 14691259
  • Triepels RH  et al. Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns. J Biol Chem 276:8892-7 (2001). PubMed: 11112787
  • Hanson BJ  et al. Cytochrome c oxidase-deficient patients have distinct subunit assembly profiles. J Biol Chem 276:16296-301 (2001). PubMed: 11278850
  • Dey R  et al. Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines. J Biol Chem 275:31520-7 (2000). PubMed: 10908562

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