Fig. 1.
Fig. 1. Flow cytometric determination of apoptosis by ISEL in antigen defined subpopulations (patient No. 24, Table 1). Peripheral lymphocytes were incubated in vitro in the presence or absence of F-ara-A (3 μmol/L) or CyA (100 ng/mL). Apoptosis was evaluated after 72 hours in CD19+, CD3+, CD4+, and CD8+ lymphocytes. The number in the top right quadrant represents the percentage of apoptotic cells in the antigen-defined population. The numbers in parentheses represent the percentage of antigen-defined apoptotic cells within the total number of peripheral lymphocytes.

Flow cytometric determination of apoptosis by ISEL in antigen defined subpopulations (patient No. 24, Table 1). Peripheral lymphocytes were incubated in vitro in the presence or absence of F-ara-A (3 μmol/L) or CyA (100 ng/mL). Apoptosis was evaluated after 72 hours in CD19+, CD3+, CD4+, and CD8+ lymphocytes. The number in the top right quadrant represents the percentage of apoptotic cells in the antigen-defined population. The numbers in parentheses represent the percentage of antigen-defined apoptotic cells within the total number of peripheral lymphocytes.

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