Considering a phenotypic assay (proliferation/viability), would you transfect together with the target gene siRNA also negative ctrl siRNAs to achieve the same concentration as the multiple target gene siRNA?

Eg: transfection of siRNA ctrl at 30 nM VS transfection of siRNA-antiA 10 nM + ctrl at 20 nM (total 30 nM) VS transfection of siRNA-antiA (10)+ antiB (10) + antiC (10). Would the three condition be comparable?

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