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Cell growth after induction. Each cell clone, as indicated at the top of each panel, was adjusted to 5 × 105 cells in 10 ml of RPMI 1640 medium on day 0 and cultured either with (closed circles) or without (open circles) 10 μM CdCl2. On each day, 1 ml of cell suspension was removed from the cultures, and the number of viable cells in the cell suspension was measured.
