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Cell death was analyzed by quantifying extracellular lactate dehydrogenase (LDH) activity with the cytotoxicity detection kit of LDH (Roche Applied Science), as described [68].
Transitivity was analyzed by quantifying possible target cleavage-derived transient siRNAs.
Formation of endothelial cell layers was analyzed by quantifying the number of endothelial cells by phase contrast microscopy.
The cell cycle was analyzed by quantifying the amount of stained DNA with flow cytometry after transfection of LNCaP cells with siPCA3 and siScr.
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The role that this necrotic response to D. dadantii inoculation might play in disease development has been analyzed by quantifying maceration symptoms, necrosis occurrence and bacterial growth in bos1 and Col-0 plants.
Results from round 1 were analyzed by quantifying scores on each item, by calculating percentages of respondents' answers and by evaluating the consensus in the answers.
Residual biofilms were analyzed by quantifying the viable cells (CFU/mL), and biofilm architecture was evaluated by confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM).
Color tone changes were analyzed by quantifying the amount of chlorophyll a and phycocyanin, as described previously (Arnon et al. 1974).
The resulting images were analyzed by quantifying the Cy3 and Cy5 fluorescence intensity at each feature on the array using the Agilent Feature Extraction Software (V10.5).
Data were analyzed by quantifying the statistical distribution (mean, median, SD, relative SD, coefficient of skewness, coefficient of kurtosis, Kolmogorov and D'Agostino Pearson test, percentiles, 95% CI).
The effects of TA on the level of crystalline cellulose in poplar cells were analyzed by quantifying glucose in the acid-insoluble fraction of the cell walls.
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