Fig. 1.
Fig. 1. Mixtures of D2 and B6 marrow maintain the parental ratio of LTC-IC in culture. / Bone marrow cells from D2, B6, and a 1:1 mixture of the marrows were plated onto S17 stroma. Between 48 and 192 wells were seeded for each cell concentration. The data depicted are from 2 independent experiments, a dashed vertical line separates different experiments. LTC-IC values (per 105 cells seeded) at 4 weeks of culture are indicated above the figure. Positive wells were then harvested and the cells from each well were stained with mAb specific for H2d (D2, white bars) and H2b (B6, black bars). Because the cells in each microculture were derived from an LTC-IC, the genotype of the differentiated progeny establishes the genotype of the LTC-IC. The plating density (cells/well), percentage negative wells, and number of wells tested for each cell dilution (n) is indicated below the figure.

Mixtures of D2 and B6 marrow maintain the parental ratio of LTC-IC in culture.

Bone marrow cells from D2, B6, and a 1:1 mixture of the marrows were plated onto S17 stroma. Between 48 and 192 wells were seeded for each cell concentration. The data depicted are from 2 independent experiments, a dashed vertical line separates different experiments. LTC-IC values (per 105 cells seeded) at 4 weeks of culture are indicated above the figure. Positive wells were then harvested and the cells from each well were stained with mAb specific for H2d (D2, white bars) and H2b (B6, black bars). Because the cells in each microculture were derived from an LTC-IC, the genotype of the differentiated progeny establishes the genotype of the LTC-IC. The plating density (cells/well), percentage negative wells, and number of wells tested for each cell dilution (n) is indicated below the figure.

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