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Error bars show two standard deviations based on triplicate analysis.
For quantitative comparisons, values were reported as mean ± SD based on triplicate analysis for each sample.
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Through quantitative analysis based on triplicate injections into the HPLC system, we found that the linearity of detection of the four compounds ranged from 2 to 500 ppm (μg/mL), with the squared correlation coefficient exceeding 0.999 in each case (Table 2).
Experiments were based on triplicate biological replicates.
All parameters were measured based on triplicate measurements.
Error bars indicate standard deviation calculated based on triplicate experiments.
All values were based on triplicate samples from which the mean and the standard error of the mean were calculated.
Data for each marker are based on triplicate cultures with ≥20 randomly chosen high power fields quantified for each staining.
Activity assignments based on triplicate runs.
Based on triplicate analyses, spots that showed a statistically significant (p-value < 0.05, One-way ANOVA) and changed ≥1.5-fold were considered for further analysis.
Expression profiling and drug predictions based on triplicate sections were analyzed.
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based on multivariate analysis
based on rigorous analysis
based on statistical analysis
based on retrospective analysis
based on biochemical analysis
based on semantic analysis
based on genomic analysis
based on detailed analysis
based on careful analysis
based on elemental analysis
based on quantitative analysis
based on structural analysis
based on morphometric analysis
based on preliminary analysis
based on combined analysis
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