Anti-Ubiquinol-Cytochrome C Reductase Core Protein I antibody [16D10AD9AH5] (ab110252)

Publishing research using ab110252? Please let us know so that we can cite the reference in this datasheet.

ab110252 has been referenced in 44 publications.

  • Kazak L  et al. UCP1 deficiency causes brown fat respiratory chain depletion and sensitizes mitochondria to calcium overload-induced dysfunction. Proc Natl Acad Sci U S A 114:7981-7986 (2017). WB ; Mouse . PubMed: 28630339
  • Hernansanz-Agustín P  et al. Mitochondrial complex I deactivation is related to superoxide production in acute hypoxia. Redox Biol 12:1040-1051 (2017). WB . PubMed: 28511347
  • Boutant M  et al. Mfn2 is critical for brown adipose tissue thermogenic function. EMBO J 36:1543-1558 (2017). PubMed: 28348166
  • Huertas JR  et al. Antioxidant effect of exercise: Exploring the role of the mitochondrial complex I superassembly. Redox Biol 13:477-481 (2017). PubMed: 28719865
  • Theisen BE  et al. Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. Am J Med Genet A 173:2505-2510 (2017). PubMed: 28650581
  • Patrinostro X  et al. Relative importance of ßcyto- and ?cyto-actin in primary mouse embryonic fibroblasts. Mol Biol Cell 28:771-782 (2017). PubMed: 28077619
  • Chen Y  et al. Synergistic Effects of Cilostazol and Probucol on ER Stress-Induced Hepatic Steatosis via Heme Oxygenase-1-Dependent Activation of Mitochondrial Biogenesis. Oxid Med Cell Longev 2016:3949813 (2016). WB . PubMed: 27057275
  • Davoudi M  et al. COX7A2L/SCAFI and Pre-Complex III Modify Respiratory Chain Supercomplex Formation in Different Mouse Strains with a Bcs1l Mutation. PLoS One 11:e0168774 (2016). PubMed: 27997587
  • Kovárová N  et al. Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects. Biochim Biophys Acta 1862:705-15 (2016). WB . PubMed: 26804654
  • Kovárová N  et al. Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect. Data Brief 7:1004-9 (2016). WB . PubMed: 27408912
  • Garaude J  et al. Mitochondrial respiratory-chain adaptations in macrophages contribute to antibacterial host defense. Nat Immunol 17:1037-1045 (2016). PubMed: 27348412
  • Sakakibara I  et al. Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle. Skelet Muscle 6:30 (2016). WB ; Mouse . PubMed: 27597886
  • Huang S  et al. 2,2',4,4'-Tetrabromodiphenyl ether injures cell viability and mitochondrial function of mouse spermatocytes by decreasing mitochondrial proteins Atp5b and Uqcrc1. Environ Toxicol Pharmacol 46:301-10 (2016). WB, IHC ; Mouse . PubMed: 27525561
  • Rajendran J  et al. Effect of High-Carbohydrate Diet on Plasma Metabolome in Mice with Mitochondrial Respiratory Chain Complex III Deficiency. Int J Mol Sci 17:N/A (2016). WB . PubMed: 27809283
  • Luna-Sánchez M  et al. The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene. EMBO Mol Med 7:670-87 (2015). PubMed: 25802402
  • 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
  • Buzelle SL  et al. The contribution of IL-6 to beta 3 adrenergic receptor mediated adipose tissue remodeling. Physiol Rep 3:N/A (2015). Mouse . PubMed: 25713332
  • Lim SC  et al. Anti-cancer analogues ME-143 and ME-344 exert toxicity by directly inhibiting mitochondrial NADH: ubiquinone oxidoreductase (Complex I). Am J Cancer Res 5:689-701 (2015). PubMed: 25973307
  • 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
  • Marine A  et al. Peroxynitrite induced mitochondrial biogenesis following MnSOD knockdown in normal rat kidney (NRK) cells. Redox Biol 2:348-57 (2014). WB . PubMed: 24563852
  • Jannig PR  et al. Autophagy signaling in skeletal muscle of infarcted rats. PLoS One 9:e85820 (2014). WB ; Rat . PubMed: 24427319
  • Ritchie IR  et al. Adiponectin is sufficient, but not required, for exercise-induced increases in the expression of skeletal muscle mitochondrial enzymes. J Physiol 592:2653-65 (2014). WB ; Mouse . PubMed: 24687585
  • Wanschers BF  et al. A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability. Hum Mol Genet N/A:N/A (2014). Human . PubMed: 25008109
  • García-Corzo L  et al. Ubiquinol-10 ameliorates mitochondrial encephalopathy associated with CoQ deficiency. Biochim Biophys Acta 1842:893-901 (2014). PubMed: 24576561
  • García-Corzo L  et al. Dysfunctional Coq9 protein causes predominant encephalomyopathy associated with CoQ deficiency. Hum Mol Genet 22:1233-48 (2013). WB . PubMed: 23255162
  • Szklarczyk R  et al. A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia. Hum Mol Genet 22:656-67 (2013). Human . PubMed: 23125284
  • Kovárová N  et al. High molecular weight forms of mammalian respiratory chain complex II. PLoS One 8:e71869 (2013). WB ; Human . PubMed: 23967256
  • Mennes E  et al. Aging-Associated Reductions in Lipolytic and Mitochondrial Proteins in Mouse Adipose Tissue Are Not Rescued by Metformin Treatment. J Gerontol A Biol Sci Med Sci N/A:N/A (2013). Mouse . PubMed: 24127429
  • Frier BC  et al. Epinephrine and AICAR-induced PGC-1a mRNA expression is intact in skeletal muscle from rats fed a high-fat diet. Am J Physiol Cell Physiol 302:C1772-9 (2012). WB ; Rat . PubMed: 22496244
  • Ye F  et al. Peroxisome proliferator-activated receptor ? (PPAR?) mediates a Ski oncogene-induced shift from glycolysis to oxidative energy metabolism. J Biol Chem 286:40013-24 (2011). WB . PubMed: 21917928
  • Frier BC  et al. Reductions in RIP140 are not required for exercise- and AICAR-mediated increases in skeletal muscle mitochondrial content. J Appl Physiol 111:688-95 (2011). WB ; Rat . PubMed: 21700896
  • Cameron JM  et al. Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes. Am J Hum Genet 89:486-95 (2011). WB ; Human . PubMed: 21944046
  • Kotarsky H  et al. Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation. Mitochondrion 10:497-509 (2010). PubMed: 20580947
  • Mayr JA  et al. Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit. Hum Mol Genet 19:3430-9 (2010). WB ; Human . PubMed: 20566710
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). WB ; Mouse . PubMed: 20100866
  • Son M  et al. Redox susceptibility of SOD1 mutants is associated with the differential response to CCS over-expression in vivo. Neurobiol Dis 34:155-62 (2009). PubMed: 19320055
  • 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
  • Leary SC & Sasarman F Oxidative phosphorylation: synthesis of mitochondrially encoded proteins and assembly of individual structural subunits into functional holoenzyme complexes. Methods Mol Biol 554:143-62 (2009). PubMed: 19513673
  • Ahn BH  et al. A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis. Proc Natl Acad Sci U S A 105:14447-52 (2008). PubMed: 18794531
  • 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
  • Minai L  et al. Mitochondrial respiratory chain complex assembly and function during human fetal development. Mol Genet Metab 94:120-6 (2008). PubMed: 18249146
  • 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
  • Honzík T  et al. Specific properties of heavy fraction of mitochondria from human-term placenta - glycerophosphate-dependent hydrogen peroxide production. Placenta 27:348-56 (2006). PubMed: 15949844
  • Mrácek T  et al. Time-course of hormonal induction of mitochondrial glycerophosphate dehydrogenase biogenesis in rat liver. Biochim Biophys Acta 1726:217-23 (2005). PubMed: 16039782


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