Fig. 4.
Fig. 4. Colony quantitation. / (A) Quantitation of myeloid colonies (CFU-G and CFU-GM) derived from the bone marrow cells of either wild type or β6I/β6I mice using growth conditions that permitted myeloid differentiation after 8 days of culture. (B) Quantitation of erythroid colonies (BFU-E) using conditions that permitted only erythroid growth after 8 days of culture. There was no significant difference in the numbers of myeloid or erythroid colonies derived from either the β6I/β6I or the βwt/βwt mice in the absence of G418. The addition of 900 μg/mL active G418 caused near-complete suppression of colony formation from wild-type bone marrow cells. In contrast, G418 did not suppress myeloid or the erythroid colony numbers (or the sizes of colonies) derived from the bone marrow cells of β6I/β6I mice. Graphs represent means and standard deviations from 3 separate experiments.

Colony quantitation.

(A) Quantitation of myeloid colonies (CFU-G and CFU-GM) derived from the bone marrow cells of either wild type or β6I6I mice using growth conditions that permitted myeloid differentiation after 8 days of culture. (B) Quantitation of erythroid colonies (BFU-E) using conditions that permitted only erythroid growth after 8 days of culture. There was no significant difference in the numbers of myeloid or erythroid colonies derived from either the β6I6I or the βwtwt mice in the absence of G418. The addition of 900 μg/mL active G418 caused near-complete suppression of colony formation from wild-type bone marrow cells. In contrast, G418 did not suppress myeloid or the erythroid colony numbers (or the sizes of colonies) derived from the bone marrow cells of β6I6I mice. Graphs represent means and standard deviations from 3 separate experiments.

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