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The effectiveness of each fuel treatment was assessed by simulating 25,000 wildfires using the MTT fire spread algorithm.
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Cell viability was measured using the MTT assay (Sigma Aldrich, Saint Louis, MO, USA).
Cell toxicity was evaluated using the MTT and LDH assay.
Instead, the inhibition of p38 inhibition seemed to decrease the metabolic activity and compromise the cellular membrane integrity, which was determined using the MTT assay and the LDH assay, respectively (Fig. 6a,b).
Cytotoxicity of Fsn0503 was determined using the MTT viability assay.
Aggregate cytotoxicity was assessed using the MTT reduction inhibition assay [65].
Tissue viability was measured at 24 hours after reperfusion using the MTT assay [9].
Cell viability was carried out using the MTT (3- 4,5-dimethylthiazol-2-yl -2,5 diphenyltetrazolium bromide) dye reduction assay [54].
Viable cell density was then assessed using the MTT (3- 4,5-dimethylthiazol-2-yl -2,5 diphenyl tetrazolium bromide) assay.
Cell viability was measured by using the MTT assay (Sigma,M5655).
The cytotoxicity assay was conducted using the MTT method as previously described.
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