NDUFS7 Polyclonal Antibody (E-AB-11433)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human ovarian cancer |
| Dilution | IHC 1:50-1:200 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human NDUFS7 |
| Abbre | NDUFS7 |
| Synonyms | CI 20, CI-20kD, Complex I 20kDa subunit, Complex I mitochondrial respiratory chain 20 KD subunit, Complex I-20kD, FLJ45860, FLJ46880, MGC120002, MY017, NADH , NADH coenzyme Q reductase, NADH dehydrogenase (ubiquinone) Fe S protein 7 20kDa (NADH coenzyme Q reductase) |
| Swissprot | |
| Cellular Localization | Mitochondrion. |
| Concentration | 0.7 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Metabolism, Neuroscience, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| 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. |
Other Clones
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Other Formats
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Unconjugated
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