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NDUFS3 encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Additionally we are shipping NDUFS3 Proteins (10) and many more products for this protein.
Showing 10 out of 80 products:
Human Monoclonal NDUFS3 Primary Antibody for IHC (p), IP - ABIN561943
Cheng, Kuo, Fan, Fang, Jiang, Lo, Wang, Kao, Lee: Overexpression of Lon contributes to survival and aggressive phenotype of cancer cells through mitochondrial complex I-mediated generation of reactive oxygen species. in Cell death & disease 2013
Human Polyclonal NDUFS3 Primary Antibody for WB - ABIN2786780
Vogel, Dieteren, van den Heuvel, Willems, Smeitink, Koopman, Nijtmans: Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits. in The Journal of biological chemistry 2007
Human Polyclonal NDUFS3 Primary Antibody for ELISA, WB - ABIN4338417
Martinvalet, Dykxhoorn, Ferrini, Lieberman: Granzyme A cleaves a mitochondrial complex I protein to initiate caspase-independent cell death. in Cell 2008
High NDUFS3 expression is associated with IgA nephropathy.
pH stability of w-t and Leigh syndrome mutant varied at extreme acidic pH. the molten globule like structure of w-t at pH1 (show AGXT Antibodies) was absent in case of the mutant protein. Both the w-t and mutant proteins showed multi-step thermal and Gdn (show SERPINE2 Antibodies)-HCl induced unfolding
NDUFS3 is down-regulated in serous ovarian adenocarcinoma
Expressions of GRIM-19 (show NDUFA13 Antibodies), NDUFS3, and extracellular matrix elements are correlated with invasive capabilities of breast cancer cell lines.
a novel, biomarker potential of a mitochondrial complex I subunit protein, NDUFS3 - as a robust indicator of breast cancer progression and invasiveness as well as of hypoxia/necrosis in clinical specimens of invasive ductal carcinoma, was uncovered.
This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.
NADH dehydrogenase (ubiquinone) Fe-S protein 3
, NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial
, NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase)
, OXPHOS complex I 30 kDa subunit
, NADH-ubiquinone oxidoreductase 30 kDa subunit
, complex I-30kD
, NADH dehydrogenase-ubiquinone 30 kDa subunit
, complex I 30kDa subunit
, mitochondrial complex I subunit NDUFS3