Fig. 2.
Fig. 2. Flow cytometric analysis of untransduced LAD CD34+ cells, transduced LAD CD34+ cells, and normal CD34+ cells. LAD CD34+ cells were transduced using the retroviral vector PG13/LgCD18 in a 3-day supernatant transduction on CH-296. Untransduced LAD CD34+ cells and normal CD34+ cells were grown for 3 days in IMDM/30% plus growth factors. After 3 days, all three cell populations were immunostained with either anti-human CD18, CD11a, or CD11b (X-axis where noted) and CD34 (Y-axis). 7AAD was used to gate out dead cells (not shown).

Flow cytometric analysis of untransduced LAD CD34+ cells, transduced LAD CD34+ cells, and normal CD34+ cells. LAD CD34+ cells were transduced using the retroviral vector PG13/LgCD18 in a 3-day supernatant transduction on CH-296. Untransduced LAD CD34+ cells and normal CD34+ cells were grown for 3 days in IMDM/30% plus growth factors. After 3 days, all three cell populations were immunostained with either anti-human CD18, CD11a, or CD11b (X-axis where noted) and CD34 (Y-axis). 7AAD was used to gate out dead cells (not shown).

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