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Supplementary Figure 1. PMN enrichment measurement by flow cytometry (n=4; representative). Supplementary Figure 1. PMN enrichment measurement by flow cytometry (n=4; representative).

Supplementary Figure 1. PMN enrichment measurement by flow cytometry (n=4; representative). - PowerPoint Presentation

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Supplementary Figure 1. PMN enrichment measurement by flow cytometry (n=4; representative). - PPT Presentation

The PMN enrichment was carried out by double gradient centrifugation A single cell suspension was 1x105 cells stained with the following markers CD15BV421 Pangranulocyte CD66bFITC Neutrophil maturity CD16APC Neutrophil FC receptor CCR3APCCy7 Eosinophil and basophil and CD56Pe ID: 1039708

pmn neutrophil cell enrichment neutrophil pmn enrichment cell cd66b cells ccr3 population plot double cd15 cd56 basophil eosinophil cd16

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1. Supplementary Figure 1. PMN enrichment measurement by flow cytometry (n=4; representative). The PMN enrichment was carried out by double gradient centrifugation. A single cell suspension was (1x10^5 cells) stained with the following markers: CD15-BV421 (Pan-granulocyte), CD66b-FITC (Neutrophil maturity), CD16-APC (Neutrophil FC receptor), CCR3-APC-Cy7 (Eosinophil and basophil), and CD56-PerCP (NK cell). PMN population was gated based on the FSC-SSC scatter plot. The CD15+ and CD66b+ double positive cells were gated using a quadrant plot. This population indicated neutrophil enrichment, which was an average of 85.45% (± 6.20%). We also looked at contaminating eosinophil/basophil (CCR3) and NK-cell (CD56) populations by plotting against CD16 (neutrophil specific), and found them to be 1.14% (± 1.02%) and 1.9% (± 2.00 %) respectively.