Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
NDUFS6 encodes a subunit of the NADH oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. Additionally we are shipping NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) Proteins (11) and many more products for this protein.
Showing 10 out of 55 products:
Human Polyclonal NDUFS6 Primary Antibody for WB - ABIN1881571
Saito, Kawamoto, Kamatani: Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects. in Journal of human genetics 2009
Show all 4 Pubmed References
Human Polyclonal NDUFS6 Primary Antibody for WB - ABIN518262
Jeon, Jeong, Baek, Koo, Park, Yang, Yu, Kim, Pak: Network clustering revealed the systemic alterations of mitochondrial protein expression. in PLoS computational biology 2011
The studies identify for the first time that complex I deficiency as the result of interruption of Ndufs6 is an independent cause of renal impairment.
Data show that Ndufs6(gt/gt (show FABP6 Antibodies)) mice are born healthy, attain normal weight and maturity, and are fertile, however, after 4 mo in males and 8 mo in females, Ndufs6(gt/gt (show FABP6 Antibodies)) mice are at increased risk of cardiac failure and death.
CD147 appears to regulate complex I activity and apoptosis in malignant melanoma cells by interacting with mitochondrial NDUFS6.
NDUFS6, a complex I subunit gene not previously associated with complex I deficiency, was grossly underexpressed in t patient cell lines.
NDUFS6 is required for the assembly and stabilization of a portion of complex I that contains a number of subunits.
This gene encodes a subunit of the NADH oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.
, NADH dehydrogenase Fe-S protein 6
, NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial
, NADH-ubiquinone oxidoreductase 13 kDa-A subunit
, complex I-13kD-A
, NADH ubiquinone oxidoreductase
, NADH:ubiquinone oxidoreductase NDUFS6 subunit
, complex I 13kDa subunit A
, complex I, mitochondrial respiratory chain, 13-kD subunit
, mitochondrial complex I subunit NDUFS6