NDUFS6 Polyclonal Antibody (E-AB-15246)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human liver cancer |
| Dilution | IHC 1:50-1:200 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human NDUFS6 |
| Abbre | NDUFS6 |
| Synonyms | 13kDa (NADH coenzyme Q reductase, BC059730, CI 13kA, CI 13kD A, CI-13kD-A, CI13KDA, Complex I 13kD A, Complex I 13kDa subunit A, Complex I mitochondrial respiratory chain 13 kD subunit, Complex I-13kD-A, IP13, MGC107676, NADH dehydrogenase (ubiquinone) Fe-S protein 6 |
| Swissprot | |
| Cellular Localization | Mitochondrion inner membrane. |
| Concentration | 0.4 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Metabolism, Signal Transduction, Tags and Cell Markers |
| 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 subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders. |
Other Clones
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Other Formats
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Unconjugated
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