Figure 7.
Figure 7. Regulation of Tie-2 receptor expression on cord blood CD34+ cells. (A) Two-color flow cytometric analysis of cord blood CD34+ cells showing expression of Tie-2 in freshly isolated cells (day 0) and after 2 days of culture (day 2). (B) Three-color flow cytometric analysis of cord blood CD34+ cells stained for CD34, CD11b, and Tie-2. Middle panels show the staining for CD34 and CD11b relative to isotype control antibodies in freshly isolated cells (day 0) and after 2 days of culture (day 2). Gating on the CD34+CD11b+ (B, upper panels) and CD34+CD11b– (B, lower panels) populations demonstrate the selective up-regulation of Tie-2 in the CD34+CD11b+ subset at 2 days of culture. Percentages of CD34+Tie-2+ cells and CD34+CD11b+ are indicated in dot-plot quadrants. Data are representative of 5 independent experiments.

Regulation of Tie-2 receptor expression on cord blood CD34+ cells. (A) Two-color flow cytometric analysis of cord blood CD34+ cells showing expression of Tie-2 in freshly isolated cells (day 0) and after 2 days of culture (day 2). (B) Three-color flow cytometric analysis of cord blood CD34+ cells stained for CD34, CD11b, and Tie-2. Middle panels show the staining for CD34 and CD11b relative to isotype control antibodies in freshly isolated cells (day 0) and after 2 days of culture (day 2). Gating on the CD34+CD11b+ (B, upper panels) and CD34+CD11b– (B, lower panels) populations demonstrate the selective up-regulation of Tie-2 in the CD34+CD11b+ subset at 2 days of culture. Percentages of CD34+Tie-2+ cells and CD34+CD11b+ are indicated in dot-plot quadrants. Data are representative of 5 independent experiments.

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