Fig. 3.
Fig. 3. Analysis of CD4 and CD34 expression on cultured CD4+ CD34++ CD38− Lin− and CD4− CD34++ CD38− Lin− LDFL cells. (A) Fetal liver cells were prepared for FACS by the method described in the legend to Table 1, with the exception that streptavidin-TC was substituted for streptavidin-APC. After 4 days of culture in KL + GM-CSF + EPO, the cultured cells were restained using the same MoAbs as used for cell sorting and analyzed using a FACScan. (B) CD4+ CD34++ CD38− Lin− and CD4− CD34++ CD38− Lin− LDFL cells, isolated by the identical procedure used in Table 1, were reanalyzed after 7 days of culture in KL + GM-CSF. CD34 expression was clearly observed to be greater on the cultured CD4+ cells than on the cultured CD4− cells.

Analysis of CD4 and CD34 expression on cultured CD4+ CD34++ CD38 Lin and CD4 CD34++ CD38 Lin LDFL cells. (A) Fetal liver cells were prepared for FACS by the method described in the legend to Table 1, with the exception that streptavidin-TC was substituted for streptavidin-APC. After 4 days of culture in KL + GM-CSF + EPO, the cultured cells were restained using the same MoAbs as used for cell sorting and analyzed using a FACScan. (B) CD4+ CD34++ CD38 Lin and CD4 CD34++ CD38 Lin LDFL cells, isolated by the identical procedure used in Table 1, were reanalyzed after 7 days of culture in KL + GM-CSF. CD34 expression was clearly observed to be greater on the cultured CD4+ cells than on the cultured CD4 cells.

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