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We evaluated cell viability and functions, and also monitored the oxygen consumption.
We evaluated cell viability at different times after transfection by performing a trypan blue exclusion test.
We incubated cells with the selected aptamers and then evaluated cell viability by the MTT method.
We evaluated cell viability after trastuzumab treatment using different breast cancer cell lines.
We evaluated cell viability with the CellTiter-Glo Luminescent Cell Viability Assay Kit (cat. NO G7571; Promega, Fitchburg, WI, USA).
We also evaluated cell viability in bone marrow stromal cells and MLO-y4 osteocytes treated with dexametasone with or without risedronate.
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3- 4,5-dimethylthiazol-2yl- -2,5-diphenyl tetrazolium bromide (MTT) assay was used to evaluate cell viability.
The methylthiazol tetrazolium (MTT) assay, a cell apoptosis study and the flow cytometry were used to evaluate cell viability of mouse fibroblast L929.
After the hyperthermia test, the cells were incubated for 24 h prior to undergoing MTT assay to evaluate cell viability.
The remaining cell solutions in cultured 96-well plate were used to evaluate cell viability by 3- 4,5-dimethylthiazole-2-yl -2,5-diphenyl tetrazolium bromide (MTT) assay.
[3- 4,5-Dimethylthiazol-2-yl -2,5-diphenyl tetrazolium bromide] (MTT) assay was used to evaluate cell viability, measuring mitochondrial dehydrogenase activity as previously described [3- 4,5-Dimethylthiazol-2-yl -2,5-diphenyl
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