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Modeling was done by software (STELLA II ® 9.1.4) and the data were processed using fourth-order Runge-Kutta Equation approximations that were incorporated into the software.
After cell staining, fluorescence was assayed using the FACSCalibur flow cytometer from BD Immunocytometry Systems and the data were processed using the Cellquest Pro and FlowJo softwares.
Subsequently, the labeled cells were analyzed by a flow cytometer and the data were processed using WinMDI 2.9 software.
Flow cytometry used BD Calibur or BD LSR Fortessa and the data were processed using FlowJo softwaree (Treestar).
All the samples were analyzed by flow cytometry (FACSCanto II, BD Biosciences) and the data were processed using FACS Diva software.
Phosphorescence emission spectra were recorded with a Horiba FluoroMax-4 spectrofluorimeter and the data were processed using the FluorEssence v3.5 software package.
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The data were processed using NMRPipe and visualized using SPARKY.
The data were processed using mathematical observers.
The data were processed using Origin 7.0.
The data were processed using Prism 3.0 software.
The data were processed using HKL2000.
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