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After 24, 48, and 72 h of exposure, viability was assessed on the basis of cellular conversion of MTT into a formazan product.
Following exposure, viability was determined using Alamar Blue reduction.
After 48 h exposure, viability, cell cycle, protein expression associated with tumor process and adhesion/invasion in matrigel were analyzed.
On the third day of PAHs exposure, viability reduced remarkably in all the cells and 2(d)).
Parallel aliquots of the cells were grown at different oxygen pressures and after 72 hours of drug exposure viability was measured with the fluorometric microculture cytotoxicity assay (FMCA).
After 72 h of exposure, viability was assessed on the basis of cellular conversion of MTT into a formazan product using the Promega CellTiter 96 nonradioactive cell proliferation assay according to the manufacturer's protocol.
Similar(54)
After chemical exposure, cell viability was analyzed by fluorescence detection of cell viability assays on a per microwell basis using a standard microarray scanner.
At 48 h post-drug exposure, cell viability was assessed by Alamar Blue, and the percentage viability was calculated as the ratio of siRNA treatment in the presence of drugs to vehicle treatment.
The data indicate that the light exposure inhibited viability more than the darkness exposure.
After compound exposure, cell viability was assessed by the commonly used MTT assay.
24 h after exposure, cellular viability (XTT) and inflammation (IL-6, IL-8 and MCP-1) were assessed.
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