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NDUFS7 encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. Additionally we are shipping NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) Proteins (9) and NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) Kits (7) and many more products for this protein.
Showing 10 out of 52 products:
Human Polyclonal NDUFS7 Primary Antibody for WB - ABIN1881572
Burkard, Planyavsky, Kaupe, Breitwieser, Bürckstümmer, Bennett, Superti-Furga, Colinge: Initial characterization of the human central proteome. in BMC systems biology 2011
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Human Polyclonal NDUFS7 Primary Antibody for IHC, ELISA - ABIN1535068
Hyslop, Duncan, Pitkänen, Robinson: Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13. in Genomics 1997
Show all 2 references for 1535068
Human Polyclonal NDUFS7 Primary Antibody for ELISA, IP - ABIN4338425
Starr, Shiels, Harris, Pattie, Pearce, Relton, Deary: Oxidative stress, telomere length and biomarkers of physical aging in a cohort aged 79 years from the 1932 Scottish Mental Survey. in Mechanisms of ageing and development 2008
Human Monoclonal NDUFS7 Primary Antibody for ELISA - ABIN531707
Andreazza, Shao, Wang, Young: Mitochondrial complex I activity and oxidative damage to mitochondrial proteins in the prefrontal cortex of patients with bipolar disorder. in Archives of general psychiatry 2010
However, similar to another family member, RdmB, it catalyzes the introduction of a hydroxyl group, in the case of NDUFAF5 (show C20orf7 Antibodies), into Arg-73 in the NDUFS7 subunit of human complex I
no active role of NDUFS7 gene in schizophrenia, was found.
A patient with Leigh syndrome (LS), born to consanguineous parents, with severe complex I defect and a novel mutation in the NDUFS7 gene subunit.
Intronic NDUFS7 gene mutation is associated with activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome
This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
, NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial
, NADH-ubiquinone oxidoreductase 20 kDa subunit
, complex I-20kD
, NADH-ubiquinone oxidoreductase Fe-S protein 7
, NADH-coenzyme Q reductase
, NADH:ubiquinone oxidoreductase PSST subunit
, PSST subunit
, complex I 20kDa subunit
, complex I, mitochondrial respiratory chain, 20-KD subunit
, mitochondrial complex I subunit NDUFS7