The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NDUFA10-20-RE | 20 (40 μL) | 200 μL |  |
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| NDUFA10-20-OR | 20 (40 μL) | 200 μL |  |
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| NDUFA10-20-GO | 20 (40 μL) | 200 μL |  |
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| NDUFA10-20-GR | 20 (40 μL) | 200 μL |  |
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| NDUFA10-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]
Gene Symbol : NDUFA10
Gene Name : NADH:ubiquinone oxidoreductase subunit A10
Chromosome : CHR 2: 240,025,401-239,892,449
Locus : 2q37.3
Alt. Genes : FEM1B
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