MitoSciences (MS130)

Complex I Enzyme Activity Dipstick Assay Kit (ab109720)

Publishing research using ab109720? Please let us know so that we can cite the reference in this datasheet.

ab109720 has been referenced in 22 publications.

  • Tonin Y  et al. Modeling of antigenomic therapy of mitochondrial diseases by mitochondrially addressed RNA targeting a pathogenic point mutation in mitochondrial DNA. J Biol Chem 289:13323-34 (2014). PubMed: 24692550
  • Yao J  et al. Potentiation of brain mitochondrial function by S-equol and R/S-equol estrogen receptor ß-selective phytoSERM treatments. Brain Res 1514:128-41 (2013). Mouse . PubMed: 23428542
  • Hong Z  et al. Role of dynamin-related protein 1 (Drp1)-mediated mitochondrial fission in oxygen sensing and constriction of the ductus arteriosus. Circ Res 112:802-15 (2013). PubMed: 23334860
  • Bär F  et al. Mitochondrial Gene Polymorphisms That Protect Mice From Colitis. Gastroenterology N/A:N/A (2013). Mouse . PubMed: 23872498
  • Machado AM  et al. Helicobacter pylori infection affects mitochondrial function and DNA repair, thus, mediating genetic instability in gastric cells. Mech Ageing Dev N/A:N/A (2013). PubMed: 24012633
  • Ceusters JD  et al. Effect of different kinds of anoxia/reoxygenation on the mitochondrial function and the free radicals production of cultured primary equine skeletal myoblasts. Res Vet Sci 95:870-8 (2013). Functional Studies ; Horse . PubMed: 24099743
  • Bull VH  et al. Sorafenib-induced mitochondrial complex I inactivation and cell death in human neuroblastoma cells. J Proteome Res 11:1609-20 (2012). PubMed: 22268697
  • Claus C  et al. Involvement of p32 and microtubules in alteration of mitochondrial functions by rubella virus. J Virol 85:3881-92 (2011). PubMed: 21248045
  • Yao J  et al. Ovarian hormone loss induces bioenergetic deficits and mitochondrial ß-amyloid. Neurobiol Aging : (2011). Mouse . PubMed: 21514693
  • Valentin-Vega YA  et al. Mitochondrial dysfunction in ataxia telangiectasia. Blood : (2011). PubMed: 22144182
  • 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
  • Calvo SE  et al. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nat Genet 42:851-8 (2010). PubMed: 20818383
  • Calvo SE  et al. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nat Genet 42:851-8 (2010). PubMed: 20818383
  • Pennington K  et al. Differential effects of wild-type and A53T mutant isoform of alpha-synuclein on the mitochondrial proteome of differentiated SH-SY5Y cells. J Proteome Res 9:2390-401 (2010). PubMed: 20334438
  • 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). Human . PubMed: 20100866
  • 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). Human . PubMed: 20100866
  • Hauben M  et al. Energy use efficiency is characterized by an epigenetic component that can be directed through artificial selection to increase yield. Proc Natl Acad Sci U S A 106:20109-14 (2009). PubMed: 19897729
  • Marusich MF  et al. Novel antibody-based strategies for the rapid diagnosis of mitochondrial disease and dysfunction. Int J Biochem Cell Biol 41:2081-8 (2009). PubMed: 19460456
  • Baughman JM  et al. A computational screen for regulators of oxidative phosphorylation implicates SLIRP in mitochondrial RNA homeostasis. PLoS Genet 5:e1000590 (2009). PubMed: 19680543
  • Willis JH  et al. Isolated deficiencies of OXPHOS complexes I and IV are identified accurately and quickly by simple enzyme activity immunocapture assays. Biochim Biophys Acta 1787:533-8 (2009). PubMed: 19041632
  • Sugiana C  et al. Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease. Am J Hum Genet 83:468-78 (2008). PubMed: 18940309
  • Bannai S & Kasuga H Anti-inflammatory drug inhibition of transport of cystine and glutamate in cultured human fibroblasts. Biochem Pharmacol 34:1852-4 (1985). PubMed: 2860907

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