Fig. 9.
Fig. 9. Induction of apoptosis in KG1 cells overexpressing thehiwi gene. / KG1 cells were transfected under mock, pCIneo empty vector, or pCIneo-hiwi conditions. Cells were harvested at 2, 8, 12, and 32 hours, washed with PBS, and resuspended in binding buffer containing Annexin V–FITC and PI. The X-axis represents log fluorescence intensity for Annexin V staining; the Y-axis represents log fluorescence intensity for PI staining. Panels A-C show flow cytometric analysis at a 2-hour time point that consists of a mock, a pCIneo empty vector, and the pCIneo-hiwi transfected KG1 cell populations. Panels D-F, G-I, and J-L show the same analysis but at 8,12, and 32 hours (respectively) after transfection.

Induction of apoptosis in KG1 cells overexpressing thehiwi gene.

KG1 cells were transfected under mock, pCIneo empty vector, or pCIneo-hiwi conditions. Cells were harvested at 2, 8, 12, and 32 hours, washed with PBS, and resuspended in binding buffer containing Annexin V–FITC and PI. The X-axis represents log fluorescence intensity for Annexin V staining; the Y-axis represents log fluorescence intensity for PI staining. Panels A-C show flow cytometric analysis at a 2-hour time point that consists of a mock, a pCIneo empty vector, and the pCIneo-hiwi transfected KG1 cell populations. Panels D-F, G-I, and J-L show the same analysis but at 8,12, and 32 hours (respectively) after transfection.

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