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Updated: Jun 14, 2025

Step-specific Sorting of Mouse Spermatids by Flow Cytometry
Published on: December 31, 2015
Cell sorting based on pulse shapes from angle resolved detection of scattered light
Daniel Kage1, Andrej Eirich2, Kerstin Heinrich1
1German Rheumatology Research Center (DRFZ) - Flow Cytometry Core Facility, Charitéplatz 1 (Virchowweg 12), 10117, Berlin, Germany.
Abstract:
Flow cytometry is a key technology for the analysis and sorting of cells or particles at high throughput. Conventional and current flow cytometry is primarily based on fluorescent stains to detect the cells of interest. However, such stains also have disadvantages, as their effect on cells must be carefully tested to avoid effects on the results of the experiments. Alternative approaches using imaging or other label-free techniques often require highly sophisticated setups, are commonly limited in resolution, and produce challenging amounts of data. Our technology exploits scattered light instead. The custom-built flow cytometry setup comprises a fiber array in forward scatter detection for angular resolution and captures the whole pulse shape with advanced signal processing. Thereby this setup enables cell analysis and sorting purely based on scattered light signals without the need for fluorescent labels. We demonstrate the feasibility of this cell sorting technology by sorting cell lines for their cell cycle stages based on scattered light. Furthermore, we demonstrate the ability to classify human peripheral blood T- and B-cell subsets.

