E-AB-15246
NDUFS6 Polyclonal Antibody
Size
£106.20
Was £118.00
- SKU:
- E-AB-15246
- Additional Names:
- 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
- Application:
- IHC
- Concentration:
- 0.4 mg/ml
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Recombinant protein of human NDUFS6
- Uniprot:
- O75380
- Synonyms:
- CI-13kA;CI-13kD-A;CI13KDA;complex I 13kDa subunit A;Complex I-13kD-A;complex I, mitochondrial respiratory chain, 13-kD subunit;MC1DN9;NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial;NADH-ubiquinone oxidoreductase 13 kDa-A subunit;NADH:ubiquinone oxidoreductase NDUFS6 subunit
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice