Figure 1.
Figure 1. Phenotypic analysis of unsorted BM CD34+ cells at day 0 and following HUBEC culture versus GM36SF alone. Human BM CD34+ cells were cultured with either HUBEC monolayers supplemented with GM36SF or GM36SF alone for 7 days (N = 3). (A) Representative phenotype of BM CD34+ cells at day 0, day 4, and day 7 of HUBEC culture, demonstrating a high percentage of CD34+CD38– cells persistent after culture. (B) Representative phenotype of BM CD34+ cells at day 0, day 4, and day 7 of culture with GM36SF alone, demonstrating nearly complete loss of CD34+CD38– cells. All cell populations were stained with anti-CD34–FITC and anti-CD38–PE antibodies and analyzed by flow cytometry. Isotype control staining for each time point is shown at top. Numbers indicate the percent of cells in each quadrant.

Phenotypic analysis of unsorted BM CD34+ cells at day 0 and following HUBEC culture versus GM36SF alone. Human BM CD34+ cells were cultured with either HUBEC monolayers supplemented with GM36SF or GM36SF alone for 7 days (N = 3). (A) Representative phenotype of BM CD34+ cells at day 0, day 4, and day 7 of HUBEC culture, demonstrating a high percentage of CD34+CD38 cells persistent after culture. (B) Representative phenotype of BM CD34+ cells at day 0, day 4, and day 7 of culture with GM36SF alone, demonstrating nearly complete loss of CD34+CD38 cells. All cell populations were stained with anti-CD34–FITC and anti-CD38–PE antibodies and analyzed by flow cytometry. Isotype control staining for each time point is shown at top. Numbers indicate the percent of cells in each quadrant.

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