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Every extract was analyzed in duplicate.
Each mutant was analyzed in duplicate in each assay, and each experiment was performed in triplicate.
Each sample type was analyzed in duplicate (n = 2) to ensure accuracy.
Each sample was analyzed in duplicate and negative controls were included in each run.
Each dilution was analyzed in duplicate Fig. 4 Correlation between log-transformed individual measurements of Aspergillus spores and absorbance readings.
For reproducibility of the results, the experiments consisted of 5 independent biological repeats and each extract was analyzed in duplicate (2 technical repeats).
Each sample was analyzed in duplicate according to manufacturer protocol.
Each sample was analyzed in duplicate in separate experiments.
(see Supplementary Figure S1) Each sample was analyzed in duplicate and the experiment was repeated twice.
Each sample was analyzed in duplicate and each PCR experiment included at least one non-template control well.
Each sample was analyzed in duplicate, and the average threshold cycle (Ct) values of each sample for GUSB, were subtracted from the average Ct values for HSP90AA1.
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