BD HorizonTM BV711 Rabbit Anti-Active Caspase-3

Description

Flow cytometric analysis of Active Caspase-3 expression by Dexamethasone-treated Mouse thymocytes. C57BL/6 Mouse thymocytes were left Untreated Left histogram or Treated Right histogram with 1 muM of Dexamethasone for 5 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet is not lot specific. Flow cytometric analysis of Active Caspase-3 expression by Camptothecin-treated Human Jurkat cells. Cells from the Human Jurkat T-cell leukemia, ATCC TIB-152 cell line were left Untreated Left histogram or Treated Right histogram with 12 muM of Camptothecin for 6 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of Active Caspase-3 expression by Dexamethasone-treated Mouse thymocytes. C57BL/6 Mouse thymocytes were left Untreated Left histogram or Treated Right histogram with 1 muM of Dexamethasone for 5 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet is not lot specific. Show More Flow cytometric analysis of Active Caspase-3 expression by Camptothecin-treated Human Jurkat cells. Cells from the Human Jurkat T-cell leukemia, ATCC TIB-152 cell line were left Untreated Left histogram or Treated Right histogram with 12 muM of Camptothecin for 6 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of Active Caspase-3 expression by Dexamethasone-treated Mouse thymocytes. C57BL/6 Mouse thymocytes were left Untreated Left histogram or Treated Right histogram with 1 muM of Dexamethasone for 5 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet is not lot specific. Flow cytometric analysis of Active Caspase-3 expression by Camptothecin-treated Human Jurkat cells. Cells from the Human Jurkat T-cell leukemia, ATCC TIB-152 cell line were left Untreated Left histogram or Treated Right histogram with 12 muM of Camptothecin for 6 hours to induce apoptosis. Cells were washed, fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and then permeabilized with BD Perm/Wash Buffer Cat. No. 554723 . The suspended cells were subsequently stained in BD Perm/Wash Buffer with BD Horizon BV711 Rabbit Anti-Active Caspase-3 antibody Cat. No. 570789/570866 at 1 mug/test. The fluorescence histograms showing Active Caspase-3 expression were derived from gated events with the forward and side light-scatter characteristics of intact single cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo Software. Data shown on this Technical Data Sheet are not lot specific.