Figure 1.
Schema for competitive engraftment RM transplantation experiments. A mobilized, autologous peripheral blood CD34+ cell apheresis product was split into 2 equal halves. Each half was transduced using a different marker (GFP or YFP). After 10 Gy of myeloablative total-body irradiation (TBI), gene-marked grafts were then delivered at the same time, either using the OIB technique or IV via a central line. Engrafted progeny were identified from the 2 different transplant methods to compare their relative contribution to hematopoiesis by using peripheral blood samples gated on granulocytes and analyzed for GFP and YPF by flow cytometry.

Schema for competitive engraftment RM transplantation experiments. A mobilized, autologous peripheral blood CD34+ cell apheresis product was split into 2 equal halves. Each half was transduced using a different marker (GFP or YFP). After 10 Gy of myeloablative total-body irradiation (TBI), gene-marked grafts were then delivered at the same time, either using the OIB technique or IV via a central line. Engrafted progeny were identified from the 2 different transplant methods to compare their relative contribution to hematopoiesis by using peripheral blood samples gated on granulocytes and analyzed for GFP and YPF by flow cytometry.

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