Fig. 3.
Fig. 3. Flow cytometric analysis and sorting windows of cells tracked with PKH26. (A) PKH26 fluorescence of freshly sorted Lin−Sca-1+c-kit+ cells stained with PKH26 on day 0. (B and C) PKH26 fluorescence of the cell populations after 7 days of suspension culture with TPO (B) or IL-6 and FL (C). Viable (PI-negative) cells were arbitarily divided into PKH26low populations (I) and PKH26highpopulations (II): BI, 89%; BII, 8%; CI, 94%; and CII, 2.7%.

Flow cytometric analysis and sorting windows of cells tracked with PKH26. (A) PKH26 fluorescence of freshly sorted LinSca-1+c-kit+ cells stained with PKH26 on day 0. (B and C) PKH26 fluorescence of the cell populations after 7 days of suspension culture with TPO (B) or IL-6 and FL (C). Viable (PI-negative) cells were arbitarily divided into PKH26low populations (I) and PKH26highpopulations (II): BI, 89%; BII, 8%; CI, 94%; and CII, 2.7%.

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