Fig. 7.
Fig. 7. Induction of apoptosis in monocytes by Deltaext-myc in the presence of M-CSF compared to GM-CSF. / Monocytes were cultured with 10% FCS IMDM containing M-CSF (10 ng/mL), GM-CSF (100 ng/mL), or M-CSF plus GM-CSF in the presence of Deltaext-myc (1 μg/mL) or purified control medium. All wells were coated with anti-myc 9E10 F(ab′)2fragments. Cells were harvested at 12 hours, washed with binding buffer, and incubated in binding buffer containing annexin V-FITC and PI. The mean and standard error of annexin V positive cells in the PI negative window for the 3 wells are shown. (*) represents statistical difference compared with respective control.

Induction of apoptosis in monocytes by Deltaext-myc in the presence of M-CSF compared to GM-CSF.

Monocytes were cultured with 10% FCS IMDM containing M-CSF (10 ng/mL), GM-CSF (100 ng/mL), or M-CSF plus GM-CSF in the presence of Deltaext-myc (1 μg/mL) or purified control medium. All wells were coated with anti-myc 9E10 F(ab′)2fragments. Cells were harvested at 12 hours, washed with binding buffer, and incubated in binding buffer containing annexin V-FITC and PI. The mean and standard error of annexin V positive cells in the PI negative window for the 3 wells are shown. (*) represents statistical difference compared with respective control.

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