Fig. 2.
Fig. 2. Changes in cell viability during the culture with or without Ub. / (A) HL-60 and KT-3 cells were resuspended in ASF103 and ASF103 containing 1 ng/mL rhIL-6, respectively, and cultured in the presence or absence of 100 μg/mL Ub for 72 hours. Changes in cell viability were quantitated by trypan blue dye exclusion method at the times indicated. The results are shown as the mean ± SD of triplicate cultures. (B) Flow cytometric analyses of HL-60 and KT-3 cells during the culture with or without Ub. The DNA content of the cultured cells was examined by PI staining and analyzed on FACSort.

Changes in cell viability during the culture with or without Ub.

(A) HL-60 and KT-3 cells were resuspended in ASF103 and ASF103 containing 1 ng/mL rhIL-6, respectively, and cultured in the presence or absence of 100 μg/mL Ub for 72 hours. Changes in cell viability were quantitated by trypan blue dye exclusion method at the times indicated. The results are shown as the mean ± SD of triplicate cultures. (B) Flow cytometric analyses of HL-60 and KT-3 cells during the culture with or without Ub. The DNA content of the cultured cells was examined by PI staining and analyzed on FACSort.

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