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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 81 products:
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
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
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