Fig. 5.
Fig. 5. Cotreatment with Smac-4 peptide enhances Epo B– or Apo-2L/TRAIL–induced apoptosis of Jurkat cells. / Jurkat cells were treated with either 10 μM of control or Smac-4 peptide for 3 hours, followed by treatment with 10 nM Epo B or 2.5 ng/mL Apo-2L/TRAIL and/or the control or Smac-4 peptide for 24 hours. Following these treatments, the percentage of apoptotic cells (hypodiploid and sub-G1 fraction) was determined by propidium iodide staining followed by flow cytometry. Values represent the mean ± SE of 3 experiments.

Cotreatment with Smac-4 peptide enhances Epo B– or Apo-2L/TRAIL–induced apoptosis of Jurkat cells.

Jurkat cells were treated with either 10 μM of control or Smac-4 peptide for 3 hours, followed by treatment with 10 nM Epo B or 2.5 ng/mL Apo-2L/TRAIL and/or the control or Smac-4 peptide for 24 hours. Following these treatments, the percentage of apoptotic cells (hypodiploid and sub-G1 fraction) was determined by propidium iodide staining followed by flow cytometry. Values represent the mean ± SE of 3 experiments.

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