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Expression level of each gene was normalized to GAPDH expression, and further normalized to control group.
Data from ITF2357 groups were normalized to control group without ITF2357.
NCR was normalized to control for each biological replicate before pooling.
Infection scores from siRNA-treated samples were normalized to control samples transfected with non-targeting siRNAs.
Unless otherwise noted, all results were normalized to control (DMSO -treated cells anDMSO -treatedn reported as average ± standard deviation.
The NCR was normalized to control for each biological replicate before pooling, and plotted as mean normalized log (NCR) ± s.d.
Water fluxes were measured at 15-min intervals at temperatures indicated in the table and all fluxes were normalized to control values at 21°C.
Colony density was normalized to control untreated samples.
Values obtained for treatment samples were normalized to control samples.
Luciferase activity was normalized to control Renilla-Luciferase activity.
Results were normalized to control cells and expressed as mean ± SD.
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