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. Author manuscript; available in PMC: 2021 Sep 30.
Published in final edited form as: Cytometry A. 2020 Jun 1;97(6):592–601. doi: 10.1002/cyto.a.24029

Fig 1.

Fig 1.

Representative data demonstrating the comparability of uncalibrated and calibrated data across flow cytometers. (A and B) the side scatter versus anti-GFP-PE fluorescence of MV-MsfGFP are shown on the LSR Fortessa and CytoFLEX S, respectively. A comparison gate is drawn from 4 × 103 to 6 × 104 SSC-H and 1 × 103 to 3 × 104 PE-A. (C and D) the scatter cross section versus anti-GFP-PE (MESF) of MV-M-sfGFP are shown on the LSR Fortessa and CytoFLEX S, respectively. A comparison gate is drawn from 1 × 103 to 1 × 104 nm2 and 20 to 400 PE MESF. (E and F) the diameter (nm) versus anti-GFP-PE (MESF) of MV-M-sfGFP are shown on the LSR Fortessa and CytoFLEX S, respectively. A comparison gate is drawn from 100 to 180 nm to and 20 to 400 PE MESF (black). A second comparison gate is drawn from 118 to 180 nm to and 50 to 400 PE MESF (red dotted). (G and H) the diameter (nm) versus anti-GFP-PE (MESF nm−2) of MV-M-sfGFP are shown on the LSR Fortessa and CytoFLEX S, respectively. A comparison gate is drawn from 100 to 180 nm to and 5 × 10−4 to 8 × 10−3 PE MESF nm−2 (black).