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The viability was evaluated by comparison with untreated cells.
The viability was evaluated based on a comparison with untreated cells.
The viability was evaluated using a WST-8 assay and an outgrowth culture.
At the end of the incubation period, the viability was evaluated through a dye uptake assay performed according to Badisa et al. [ 13].
The parasites were used within 30 40 min of their removal from the mice peritoneal cavity and the viability was evaluated using the trypan blue dye-exclusion test.
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The cell viability was evaluated via the trypan-blue exclusion test using the Luna Cell Counter (Logos Biosystems, Gyunggi-Do, Korea).
The cell viability was evaluated using the MTT assays.
The cell viability was evaluated by the reduction of water soluble 3- 4,5-dimethylthiazol-2-yl -2,5-diphenyl tetrazolium bromide (MTT, Sigma Aldrich) to water-insoluble formazan crystals by mitochondrial dehydrogenase[88].
TSM1 and primary cultures of neuronal cells were incubated in the presence of increasing concentrations of MPP+ iodide (from 0.1 to 2 mM) for 15 h and the cell viability was evaluated using the colorimetric MTS assay (Figure 2A).
The cell viability was evaluated using the MTT method.
After culturing for 24 h at 37°C in 5% CO2 atmosphere, the cell viability was evaluated using the cell proliferation reagent WST-1 (Dojindo, Japan), according to the manufacturer's instructions.
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