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All biological replicates were run in triplicate for each transcript.
Three biological replicates were run for each condition.
These two biological replicates were run twice using this setup as technical replicates.
For each sample, three biological replicates were run alongside three technical replicates of the standard curves.
Three biological replicates were run for each isolate (except A-2A, for which one run failed).
Three independent biological replicates were run and the significance was determined with SPSS software (p < 0.05).
Three biological replicates were run in triplicates each and means and standard deviations were calculated.
Three independent biological replicates were run and the significance was determined with SPSS (p < 0.05).
Four biological replicates were run, each sampled from 15 individual plants.
Three biological replicates were run in duplicate for each dose and assay.
Two biological replicates were run for both male and female cDNA samples and each sample was technically duplicated.
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