|Click this icon to add products to compare list. Select up to 10 products.|
The detection of binding activity of Apopxin Green and phosphatidylserine in Jurkat cells. Jurkat cells were treated ithout (A, and C-Blue line) or with 20 uM camptothecin (B and C-Red line) in a 37°C, 5% CO2 incubator for 4-5 hours, and then dye loaded with Apopxin Green and Propidium Iodide for 30 minutes. The fluorescence intensity of Apopxin Green was measured with a FACSCalibur flow cytometer using the FL1 channel and the fluorescence intensity of Propidium Iodide was measured using the FL2 channel.