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A leukapheresis sample was labeled with MACS ® GMP CD62L-PE, CD3-VioGreen™ and MACS ® GMP CD8-APC for gating purposes. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. Viable lymphocytes were further gated on CD3 + cells. |
MACS ® GMP CD62L Fluorescent Antibodies Figure 1A leukapheresis sample was labeled with MACS ® GMP CD62L-PE, CD3-VioGreen™ and MACS ® GMP CD8-APC for gating purposes. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. Viable lymphocytes were further gated on CD3 + cells. |
A leukapheresis sample was labeled with MACS ® GMP CD62L-PE, CD3-VioGreen™ and MACS ® GMP CD8-APC for gating purposes. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. Viable lymphocytes were further gated on CD3 + cells. |
MACS ® GMP CD62L Fluorescent Antibodies Figure 1A leukapheresis sample was labeled with MACS ® GMP CD62L-PE, CD3-VioGreen™ and MACS ® GMP CD8-APC for gating purposes. Cells were analyzed by flow cytometry using the MACSQuant ® Analyzer 10. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. Viable lymphocytes were further gated on CD3 + cells. |
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