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Variation between triplicates was set to a maximum of 20%.
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Triplicates were set up for each group.
Average cell viability of triplicates and standard deviation between triplicates was calculated.
Deviation between triplicates was <10% for any reported value.
Each condition was set up in triplicates.
Each sample was set up in triplicate and normalized to RPS17 or 18 S expression by the DDCt method.
Each condition was set up in triplicate.
Each primer/cDNA set was set up in triplicate.
Each experimental condition was set up in triplicate wells.
The experiment was performed in triplicate and to normalize the data between experiments, the average of all ratios in each experiment was set to one.
Triplicate wells were set up.
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