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This assay determines viable cell numbers and is based on the mitochondrial conversion of the tetrazolium salt, 3 4, 5-dimethylthiazol-2-yl -2, 5-dimethylthiazol-2-yl -2ide 5-dimethylthiazol-2-yl -2; Park et al. 2005-dimethylthiazol-2-yl -2
This assay determines cell viability by measuring the absorbance of the formazan product produced by viable cells rather than detecting cellular adenosine 5'-triphosphate (ATP) levels through the use of firefly luciferase.
This assay determines apoptosis by measuring mono- and oligonucleosomes in the lysates of apoptotic cells.
This assay determines NO based on the enzymatic conversion of nitrate to nitrite by nitrate reductase.
This assay determines the total NO based on the enzymatic conversion of nitrate to nitrite by nitrate reductase.
This assay determines the appropriate amount of antibiotic sufficient to kill all cells without the cells developing antibiotic resistant properties.
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Use of this assay determined whether the presence of KSHV mirrored KS risk in different populations.
This assay determined the median amount of DNA per specimen as 5.4 ng (Additional file 2: Table S2) corresponding to a median of around 900 cells per LCM specimen.
A conservative cutoff optical density (OD) of 0.33 was used for this assay, determined by calculating the mean OD in the indirect assay of samples negative in the Wantai total assay, removing outliers, rederiving the mean negative OD, and using 1.5 × derived mean as cutoff.
In comparison with methods described earlier, this modified assay determines the repair capacity of different skin cell types to screen potential cosmetic ingredients.
This homogeneous colorimetric assay determines the number of viable cells in either PA-treated or untreated conditions.
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