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In every case, tumor cellularity was calculated using the proposed formulas by Atuegwu et al. In every case, also tumor cell count was estimated on histopathological specimens as an average cell count per 2 to 5 high-power fields.
The average cell count of each day was used to determine growth curves and doubling time.
Results were expressed as average cell count per field.
Values are given as average cell count of five high-powered fields (5 HPF).
The cells/ml was calculated as average cell count x dilution factor x 10 cells/ml.
Brazilian red propolis, the 100 μg/mL concentration showed the highest average cell count at 48 h (Fig. 6a).
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The average cell counts obtained from the Zinc/ FJB groups were compared using Students t-test.
To assess relative differences between SP and SN subjects, we computed the ratios of the average cell counts for these subgroups (SN to SP) within each age range and compartment.
Multiple-year Karenia brevis cell counts were determined on a nearly daily basis at two designated sampling sites in the waters adjacent to Mote Marine Laboratory (Bay Dock: lat./long. 27.33253/-82.57783 aNewNew Pass: lat./long. 27.33382/-82.57911) (Figure 1) and average cell counts served as proxy indicators of HAB activity within the bay.
Average cell counts were used to produce growth curves, from which cell doubling time was calculated.
Control cells, 26r, were split on day 2. Average cell counts from two independent experiments were plotted.
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