Flow cytometry is evolving — not just in dimension, but in depth. What once relied on limited detection channels and abstract readouts is now redefined by two transformative approaches: spectral cytometry and imaging cytometry.

Spectral technology captures the full emission profile of each fluorophore, unlocking the potential to analyze over 40 markers simultaneously. With automated autofluorescence extraction, rare event resolution, and reproducible, high-throughput performance, it brings high-dimensional immunophenotyping and translational research to a new level of clarity and flexibility.

Meanwhile, imaging cytometry takes us even further — from interpreting signals to visualizing biology in motion. By collecting real, high-resolution images of every cell in flow, it reveals subcellular localization, co-localization, morphology, and internalization events with exceptional accuracy. It's not about inferring complexity — it’s about seeing it.

Together, these technologies offer an unprecedented view of cellular identity and behavior, combining statistical power with spatial truth.

Not just more data — more meaning.

Not just evolution — a new language for decoding life at single-cell resolution.