Fig 6. The CD41⁺/CD61⁺ double-positive particles were separated with PLT-F reagents.

The mixture of platelets and fragmented erythrocytes that were stained with both FITC-labeled and PE-labeled antibodies were then stained with the PLT-F reagents and examined by flow cytometry. (A) The mixture was stained with both platelet-specific antibodies (anti-CD41 or anti-CD61, left) and PLT-F reagents (middle). (B) FITC-control IgG or (C) PE-control IgG was used as a negative control for fluorescence compensation.