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NDUFS7 Polyclonal Antibody, 100μg, (ATB-T3021)

$199.00
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Background: 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. [provided by RefSeq, Jul 2008]Product datasheet: Overview Product Description NDUFS7 Polyclonal Antibody, 100μg, (ATB-T3021) Species Reactivities Human,Mouse,Rat Immunogen Synthesized peptide derived from the C-terminal region of human NDUFS7. Properties Form Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. Storage Instructions-20°C/1 year References: No association between genetic polymorphisms of the NDUFS7 gene and schizophrenia in Han Chinese. Ma L, et al. Psychiatr Genet, 2013 Feb. PMID 22935918 Mitigation of NADH: ubiquinone oxidoreductase deficiency by chronic Trolox treatment. Koopman WJ, et al. Biochim Biophys Acta, 2008 Jul-Aug. PMID 18435906 A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome. Lebon S, et al. Mol Genet Metab, 2007 Sep-Oct. PMID 17604671 A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome. Lebon S, et al. Mol Genet Metab, 2007 Apr. PMID 17275378 Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. Ugalde C, et al. Hum Mol Genet, 2004 Oct 15. PMID 15317750

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NDUFS7 Polyclonal Antibody, 100μg, (ATB-T3021)
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