Quantifying cytostatic and cytotoxic outcomes of cells responding to perturbagens is an essential component of mechanism-based studies and pharmacological screening approaches. We recently described an easy and versatile method for single-cell and population-level analyses using real-time kinetic labeling (SPARKL). This technology enables zero-handling, non-disruptive protocols for integrating proliferation profiles with cell death mechanisms, along with advanced mathematics for robust analyses.
Keywords: Apoptosis; SPARKL; cell death; ferroptosis; high-throughput; kinetics; live-cell imaging; necroptosis; proliferation; real-time analysis.
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