NDUFA12 抗体
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))
This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012].
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Latest Publications for our NDUFA12 抗体
: "Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells." in: Nature methods, Vol. 10, Issue 4, pp. 315-23, (2013) (PubMed).
Aliases for NDUFA12 抗体
NADH:ubiquinone oxidoreductase subunit A12 (Ndufa12) 抗体NADH:ubiquinone oxidoreductase subunit A12 (NDUFA12) 抗体
NADH:ubiquinone oxidoreductase subunit A12 (ndufa12) 抗体
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 (ndufa12) 抗体
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 (Ndufa12) 抗体
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