05 cells and incubated for 48 h in complete medium. The cells were transfected with 8 ml of siRNA specific for human Bax or control siRNA using the siRNA BMS-345541 web transfection reagent as per the manufacturer’s instruction. 12 h after transfection, transfection medium was replaced with fresh medium containing serum and allowed to grow for 24 h. Whole cell extract was prepared 48 h after transfection for analysis of silencing efficiency by western blot using antibody against Bax. In a separate experiment, cells after 24 h of transfection were either treated with DMSO or FAE 100 mg/ml for 48 h. Then the cells were processed for chromatin condensation analysis after staining the cells with Hoechst 33342. Evaluation of Mitochondrial Membrane Potential and Chromatin Condensation In order to detect mitochondrial membrane potential loss and chromatin condensation simultaneously, we have employed dual staining of cells with mitochondrial membrane potential specific dye TMRM and nuclear stain Hoechst 33342. Briefly, the cells after treatment with FAE were stained with 50 nM of TMRM and 0.5 mg/ml of Hoechst 33342 for 15 mins. Then the cells were imaged under fluorescent microscope using DAPI and Rhodamine filter sets using 406 objective. The images were captured with Retiga Exi camera using PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22205030 NIS element software. Western Blot Cells were washed with PBS and lysed using RIPA buffer containing protease inhibitor cocktail. Briefly, equal amount of protein as determined by Bradford assay was subjected to SDS-PAGE, followed by transfer to nitrocellulose membrane. The membrane was then blocked in 5% powdered non-fat milk Tris solution for 1 h. Membrane was then incubated overnight with primary antibody, followed by incubation with species-specific horseradish peroxide conjugated secondary antibody at room temperature for 1 h. Protein bands were visualised on X-ray film using ECL-plus reagents. The primary antibodies Live Cell Caspase Analysis by FRET The breast cancer cell line MCF-7 expressing FRET based Caspase sensor, ECFP-DEVD-EYFP was employed for monitoring Caspase activation in live cells. The development of the stable cell line and imaging conditions were reported previously. For the analysis of Caspase activation, the above cell line was seeded at a density of 2000 cells/well in 96 well plates and allowed to grow for 24 h. The cells were incubated with increasing concentration of the extract for 24 h followed by ratio imaging using CARV confocal imager as described previously. Bax Mediated Apoptotic Effect of FAE were: Caspase 8, Caspase 9, PARP, Caspase 7, Bax and b-actin. FAE and imaged for TMRM, ECFP, EYFP-FRET in a time-lapse mode at an interval of 5 mins as described. The merged image of TMRM, ECFP, EYFP-FRET from the time lapse images are shown. Video S2 MCF-7 cells expressing Caspase FRET probe was stained with TMRM and exposed to 100 mg/ml of Detection of Intracellular ROS For detection of intracellular ROS generation, ROS specific fluorescent probe H2-DCF-DA was employed as per the manufacturer’s protocol. Briefly, after treating the cells with indicated concentration of drug, the cells were 
removed by mild trypsinisation and immediately washed with serum containing medium. Then the cells were loaded with 10 mM H2-DCF-DA, incubated at 37uC for 30 min, in serum free OptiMEM and immediately analyzed by flow cytometry. For ROS inhibition analysis, cells were pre-treated with 5 mM NAC for 1 h followed by drug treatment. The cells were stained with Ho
