NADH Dehydrogenase 4 (ND4)
[Edit]MT-ND4; MTND4; NAD4; NADH-Ubiquinone Oxidoreductase Chain 4; Mitochondrially Encoded NADH Dehydrogenase 4
The MT-ND4 gene provides instructions for making a protein called NADH dehydrogenase 4. This protein is part of a large enzyme complex known as complex I, which is active in mitochondria. Mitochondria are structures within cells that convert the energy from food into a form that cells can use. These cellular structures produce energy through a process called oxidative phosphorylation, which uses oxygen and simple sugars to create adenosine triphosphate, the cell's main energy source. Several mutations in the MT-ND4 gene are known to cause Leber hereditary optic neuropathy. Each of these mutations changes a single protein building block in the NADH dehydrogenase 4 protein. One MT-ND4 mutation is the most common cause of Leber hereditary optic neuropathy; it is responsible for about 70 percent of all cases worldwide.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant NADH Dehydrogenase 4 (ND4) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to NADH Dehydrogenase 4 (ND4) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to NADH Dehydrogenase 4 (ND4) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for NADH Dehydrogenase 4 (ND4) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for NADH Dehydrogenase 4 (ND4) | ELISA Kit Customized Service Offer |
Organism species: Mus musculus (Mouse)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant NADH Dehydrogenase 4 (ND4) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to NADH Dehydrogenase 4 (ND4) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to NADH Dehydrogenase 4 (ND4) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for NADH Dehydrogenase 4 (ND4) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for NADH Dehydrogenase 4 (ND4) | ELISA Kit Customized Service Offer |
Organism species: Rattus norvegicus (Rat)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant NADH Dehydrogenase 4 (ND4) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to NADH Dehydrogenase 4 (ND4) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to NADH Dehydrogenase 4 (ND4) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for NADH Dehydrogenase 4 (ND4) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for NADH Dehydrogenase 4 (ND4) | ELISA Kit Customized Service Offer |
- "Sequence and organization of the human mitochondrial genome."Nature 290:457-465(1981) [PubMed] [Europe PMC] [Abstract]
- "Differentiation of HT-29 human colonic adenocarcinoma cells correlates with increased expression of mitochondrial RNA: effects of trehalose on cell growth and maturation."Cancer Res. 52:3718-3725(1992) [PubMed] [Europe PMC] [Abstract]
- "Mitochondrial genome diversity of native Americans supports a single early entry of founder populations into America."Am. J. Hum. Genet. 71:187-192(2002) [PubMed] [Europe PMC] [Abstract]
- "Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J."Mol. Biol. Evol. 20:2132-2142(2003) [PubMed] [Europe PMC] [Abstract]
- "Mitochondrial genome variation and the origin of modern humans."Nature 408:708-713(2000) [PubMed] [Europe PMC] [Abstract]
- "Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines."Genome Res. 13:1600-1606(2003) [PubMed] [Europe PMC] [Abstract]
- "Single nucleotide polymorphisms over the entire mtDNA genome that increase the power of forensic testing in Caucasians."Int. J. Legal Med. 118:137-146(2004) [PubMed] [Europe PMC] [Abstract]
- "Mitochondrial DNA sequences of primates: tempo and mode of evolution."J. Mol. Evol. 18:225-239(1982) [PubMed] [Europe PMC] [Abstract]
- "Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase."Nature 314:592-597(1985) [PubMed] [Europe PMC] [Abstract]
- "The subunit composition of the human NADH dehydrogenase obtained by rapid one-step immunopurification."J. Biol. Chem. 278:13619-13622(2003) [PubMed] [Europe PMC] [Abstract]
- "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
- "Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy."Science 242:1427-1430(1988) [PubMed] [Europe PMC] [Abstract]
- "Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)."FEBS Lett. 292:289-292(1991) [PubMed] [Europe PMC] [Abstract]
- "Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy."Hum. Genet. 88:98-100(1991) [PubMed] [Europe PMC] [Abstract]
- "Normal variants of human mitochondrial DNA and translation products: the building of a reference data base."Hum. Genet. 88:139-145(1991) [PubMed] [Europe PMC] [Abstract]
- "A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I."Am. J. Hum. Genet. 51:457-468(1992) [PubMed] [Europe PMC] [Abstract]
- "Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia."Am. J. Hum. Genet. 58:703-711(1996) [PubMed] [Europe PMC] [Abstract]
- "Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations."Hum. Mutat. Suppl. 1:S271-S274(1998) [PubMed] [Europe PMC] [Abstract]
- "High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency."Nat. Genet. 42:851-858(2010) [PubMed] [Europe PMC] [Abstract]