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The cytotoxic effects of the tested compounds are then measured using crystal violet staining viability assay.
Carriers were sampled out (in triplicate) at the same time points from iCELLis Nano and commercially available packed bed bioreactor systems and the cell counts were measured using crystal violet staining.
Cell survival was measured using crystal violet staining, total cell count under light microscope, Annexin V and caspase-3 activation assays.
Bacteria were inoculated at an initial turbidity at 600 nm of 0.05 in all media at 37°C or 30°C for 4 h, 7 h, 15 h, and 24 h without shaking, then the growth (turbidity at 620 nm) and total biofilm were measured using crystal violet staining.
Cell growth was measured using crystal violet assay.
The cytostatic and/or cytotoxic effects were measured using crystal violet staining as described [ 18].
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The precision of the Reuters/Ipsos online polls is measured using a credibility interval.
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