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Flow cytometric analysis of human Jurkat cells stained with BD Horizon™ Fixable Viability Stain 440UV. Cells from the human Jurkat (Acute T cell leukemia, ATCC TIB-152) cell line were treated with 0.025% DMSO (Left Panels) or 5 μM camptothecin (Right Panels) for 16 hours and then stained (Bottom Panels) with BD Horizon™ Fixable Viability Stain 440UV (Cat. No. 566332) in serum-free buffer. The cells were then either left unfixed (solid line histograms) or fixed in BD Cytofix™ Fixation Buffer (Cat. No. 554655) and permeabilized in BD Phosflow™ Perm/Wash Buffer I (Cat. No. 557885) (dashed line histograms). Dead cell fluorescence is retained after fixation and permeabilization. The shift in the fluorescence of the live cells is due to a shift in auto-fluorescence post-fixation, as evidenced by the shift in the unstained (Top Panels) samples. Histograms were derived from gated events with the forward and side light-scattering characteristics of intact Jurkat cells. Flow cytometric analysis was performed using a BD LSRFortessa™ X-20 Flow Cytometry System. Please note that FVS440UV is also compatible with BD Phosflow™ Perm Buffer III (Cat. No.558050) or BD Pharmingen™ Transcription Factor Buffer Set (Cat. No. 562574/562725).