The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NDUFA2-20-RE | 20 (40 μL) | 200 μL |  |
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| NDUFA2-20-OR | 20 (40 μL) | 200 μL |  |
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| NDUFA2-20-GO | 20 (40 μL) | 200 μL |  |
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| NDUFA2-20-GR | 20 (40 μL) | 200 μL |  |
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| NDUFA2-20-AQ | 20 (40 μL) | 200 μL |  |
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The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Gene Symbol : NDUFA2
Gene Name : NADH:ubiquinone oxidoreductase subunit A2
Chromosome : CHR 5: 140,647,784-140,645,362
Locus : 5q31.3
Alt. Genes : RAD50
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