Fig. 1.
Fig. 1. Growth rate and the doubling time of Lin− Rholow/Holow cells incubated in the presence of medium containing IL-3, IL-6, IL-11, and SCF. Immediately after their purification, Lin− Rholow/Holow cells were suspended at 10 × 103 cells/mL in medium containing 4 cytokines and incubated at 37°C in a 5% CO2 containing humidified incubator as described in the Materials and Methods. At indicated intervals, duplicate aliquots of cells from growing culture were counted using a hemocytometer. The numbers in the parentheses of the insert indicate the number of experiments from which the values for that particular time point were obtained.

Growth rate and the doubling time of Lin Rholow/Holow cells incubated in the presence of medium containing IL-3, IL-6, IL-11, and SCF. Immediately after their purification, Lin Rholow/Holow cells were suspended at 10 × 103 cells/mL in medium containing 4 cytokines and incubated at 37°C in a 5% CO2 containing humidified incubator as described in the Materials and Methods. At indicated intervals, duplicate aliquots of cells from growing culture were counted using a hemocytometer. The numbers in the parentheses of the insert indicate the number of experiments from which the values for that particular time point were obtained.

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