Fig. 3.
Fig. 3. Analysis of the cell composition of individual clones derived from the CD34+CD41− and CD34+CD41+CD42− cells derived from cord blood at day 11 of culture. / The results presented are those obtained from 4 independent experiments that have been pooled, representing analysis of 112 and 95 clones, respectively. Culture conditions were serum-free plus a combination of cytokines (PEG-rHuMGDF, SCF, Epo, G-CSF, IL-3, and IL-6). Only clones having more than 200 cells were analyzed on the expression of CD15, CD41, and GPA in triple-staining experiments by means of flow cytometry. Each cell type was identified on the basis of phenotypic and scatter properties.

Analysis of the cell composition of individual clones derived from the CD34+CD41 and CD34+CD41+CD42 cells derived from cord blood at day 11 of culture.

The results presented are those obtained from 4 independent experiments that have been pooled, representing analysis of 112 and 95 clones, respectively. Culture conditions were serum-free plus a combination of cytokines (PEG-rHuMGDF, SCF, Epo, G-CSF, IL-3, and IL-6). Only clones having more than 200 cells were analyzed on the expression of CD15, CD41, and GPA in triple-staining experiments by means of flow cytometry. Each cell type was identified on the basis of phenotypic and scatter properties.

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