Abstract:Imaging Flow Cytometry (IFC) enables rapid acquisition of thousands of single-cell images per second, capturing information from multiple fluorescent channels. However, the conventional process of staining cells with fluorescently labeled conjugated antibodies for IFC analysis is labor-intensive, costly, and potentially detrimental to cell viability. To streamline experimental workflows and reduce expenses, it is imperative to identify the most relevant channels for downstream analysis. In this study, we prese… Show more
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