

567036 · 100 Tests
BDB Bioscience · Cat: 567036
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Flow cytometric analysis of CD107a expression in Jurkat cells. Jurkat cells were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and were then washed and stained in BD Perm/Wash Buffer Cat. No. 554723 with either BD Horizon R718 Mouse IgG1, kappa Isotype Control Cat. No. 566928; dashed line histogram or BD Horizon R718 Mouse Anti-Human CD107a antibody Cat. No. 567036/567220; solid line histogram . The fluorescence histogram showing CD107a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact Jurkat cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Flow cytometric analysis of CD107a expression in Jurkat cells. Jurkat cells were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and were then washed and stained in BD Perm/Wash Buffer Cat. No. 554723 with either BD Horizon R718 Mouse IgG1, kappa Isotype Control Cat. No. 566928; dashed line histogram or BD Horizon R718 Mouse Anti-Human CD107a antibody Cat. No. 567036/567220; solid line histogram . The fluorescence histogram showing CD107a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact Jurkat cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of CD107a expression in Jurkat cells. Jurkat cells were fixed with BD Cytofix Fixation Buffer Cat. No. 554655 and were then washed and stained in BD Perm/Wash Buffer Cat. No. 554723 with either BD Horizon R718 Mouse IgG1, kappa Isotype Control Cat. No. 566928; dashed line histogram or BD Horizon R718 Mouse Anti-Human CD107a antibody Cat. No. 567036/567220; solid line histogram . The fluorescence histogram showing CD107a expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of intact Jurkat cells. Flow cytometry and data analysis were performed using a BD LSRFortessa Cell Analyzer System and FlowJo software.