Complex IV Human Enzyme Activity Dipstick Assay Kit

Name Complex IV Human Enzyme Activity Dipstick Assay Kit
Supplier Abcam
Catalog ab109876
Prices $354.00, $627.00
Sizes 30 tests, 90 tests
Assay Type Sandwich (quantitative)
Sample Type Cell culture extracts, Tissue
Format Reagents
Applications FA
Species Reactivities Bovine, Human
Gene COX1
Supplier Page Shop

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Product References

Molecular diagnosis of infantile mitochondrial disease with targeted - Molecular diagnosis of infantile mitochondrial disease with targeted

Calvo SE, Compton AG, Hershman SG, Lim SC, Lieber DS, Tucker EJ, Laskowski A, Garone C, Liu S, Jaffe DB, Christodoulou J, Fletcher JM, Bruno DL, Goldblatt J, Dimauro S, Thorburn DR, Mootha VK. Sci Transl Med. 2012 Jan 25;4(118):118ra10.

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular - FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular

Fassone E, Duncan AJ, Taanman JW, Pagnamenta AT, Sadowski MI, Holand T, Qasim W, Rutland P, Calvo SE, Mootha VK, Bitner-Glindzicz M, Rahman S. Hum Mol Genet. 2010 Dec 15;19(24):4837-47.

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in - High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in

Calvo SE, Tucker EJ, Compton AG, Kirby DM, Crawford G, Burtt NP, Rivas M, Guiducci C, Bruno DL, Goldberger OA, Redman MC, Wiltshire E, Wilson CJ, Altshuler D, Gabriel SB, Daly MJ, Thorburn DR, Mootha VK. Nat Genet. 2010 Oct;42(10):851-8.

Novel antibody-based strategies for the rapid diagnosis of mitochondrial disease - Novel antibody-based strategies for the rapid diagnosis of mitochondrial disease

Marusich MF, Murray J, Xie J, Capaldi RA. Int J Biochem Cell Biol. 2009 Oct;41(10):2081-8. doi:

A computational screen for regulators of oxidative phosphorylation implicates - A computational screen for regulators of oxidative phosphorylation implicates

Baughman JM, Nilsson R, Gohil VM, Arlow DH, Gauhar Z, Mootha VK. PLoS Genet. 2009 Aug;5(8):e1000590.

Isolated deficiencies of OXPHOS complexes I and IV are identified accurately and - Isolated deficiencies of OXPHOS complexes I and IV are identified accurately and

Willis JH, Capaldi RA, Huigsloot M, Rodenburg RJ, Smeitink J, Marusich MF. Biochim Biophys Acta. 2009 May;1787(5):533-8.

Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal - Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal

Sugiana C, Pagliarini DJ, McKenzie M, Kirby DM, Salemi R, Abu-Amero KK, Dahl HH, Hutchison WM, Vascotto KA, Smith SM, Newbold RF, Christodoulou J, Calvo S, Mootha VK, Ryan MT, Thorburn DR. Am J Hum Genet. 2008 Oct;83(4):468-78.