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All data will be analyzed in duplicate by two blinded analysts.
Theoretically, to estimate intra-and inter-run accuracy and stability, five different validation samples should be analyzed in duplicate or more in at least six different runs.
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All samples were analyzed in duplicate.
Sample wines were analyzed in duplicate by trained panelists over five sessions using a balanced, complete block design.
All samples were analyzed in duplicate, and randomly selected samples were subsampled for 10 replicate analyses to monitor efficiency of homogenization and result reproducibility.
Every extract was analyzed in duplicate.
Additionally, a number of samples were analyzed in duplicate.
Each sample was analyzed in duplicate and negative controls were included in each run.
Each sample type was analyzed in duplicate (n = 2) to ensure accuracy.
All samples were analyzed in duplicate, including CuO oxidation, extraction, and quantification.
Each dilution was analyzed in duplicate Fig. 4 Correlation between log-transformed individual measurements of Aspergillus spores and absorbance readings.
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