NDUFS6 Polyclonal Antibody

Rs. 16,500.00
SKU E-AB-15246


Synonyms 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 6,13kDa (NADH coenzyme Q reductase),NADH dehydrogenase [ubiquinone] iron sulfur protein 6,mitochondrial,NADH dehydrogenase [ubiquinone] iron-sulfur protein 6,mitochondrial,NADH ubiquinone oxidoreductase 13 kDa A subunit,NADH-ubiquinone oxidoreductase 13 kDa-A subunit,NADH:ubiquinone oxidoreductase NDUFS6 subunit,NADH:ubiquinone oxidoreductase subunit S6,Ndufs6,NDUS6
Swissprot O75380
Source Rabbit
Reactivity Human,Mouse,Rat
Immunogen Recombinant protein of human NDUFS6
Application IHC,ELISA
Recommended dilution IHC 1:50-1:200
Concentration 0.4mg/mL
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
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.


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