Fig. 7.
Fig. 7. Growth kinetics of the parental MEL-B8/3 cells and transfectants of the mutant PU.1/Spi-1 genes under various culture conditions. Parental MEL-B8/3 cells (•), PU.1-Δ E-sense clone 1 cells (▪), PU.1-Δ E-antisense clone 1 cells (□), PU.1-Δ A-sense clone 1 cells (▴), and PU.1-Δ A-antisense clone 1 cells (▵) were cultured in the ordinary medium (A), in the medium containing 1.5% DMSO (B), in the medium containing 100 μmol/L ZnCl2 (C), or in the medium containing 1.5% DMSO and 100 μmol/L ZnCl2 (D). Cells (2 × 106) were placed in 10 mL of the culture medium and the cell number was determined every 24 hours. Mean values and standard deviations of three independent experiments are shown.

Growth kinetics of the parental MEL-B8/3 cells and transfectants of the mutant PU.1/Spi-1 genes under various culture conditions. Parental MEL-B8/3 cells (•), PU.1-Δ E-sense clone 1 cells (▪), PU.1-Δ E-antisense clone 1 cells (□), PU.1-Δ A-sense clone 1 cells (▴), and PU.1-Δ A-antisense clone 1 cells (▵) were cultured in the ordinary medium (A), in the medium containing 1.5% DMSO (B), in the medium containing 100 μmol/L ZnCl2 (C), or in the medium containing 1.5% DMSO and 100 μmol/L ZnCl2 (D). Cells (2 × 106) were placed in 10 mL of the culture medium and the cell number was determined every 24 hours. Mean values and standard deviations of three independent experiments are shown.

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