Topics Covered:
See inside the instrument – Break down how lasers, optics, fluidics, and detectors work together so you can troubleshoot and speak the same language as service engineers and QA auditors.
Choose the right light – Compare gas- versus diode-based lasers and learn practical rules-of-thumb for matching the best excitation source to your fluorochromes and budget.
Build smarter panels – Practice selecting dichroics and band-pass filters that keep spillover low and signal high, setting you up for cleaner multicolor data.
Control your stream – Apply fluidics principles that ensure tight core alignment and stable flow rates—essentials for reproducible cell-therapy assays.
Pick the optimal detector – Understand when classic PMTs or newer APDs deliver better sensitivity for rare-event and high-parameter CGT workflows.
Unlock spectral power – Discover how full-spectrum unmixing expands multiplexing and resolution, and learn strategies to avoid common pitfalls.
Optimize like a pro – Use best-practice checklists for voltage titration, compensation/unmixing, and panel design to shorten your assay-development timeline.
Shop with confidence – Translate technical specs into purchasing criteria so you can justify—or challenge—capital-equipment decisions.
Validate your skills – Pass the end-of-course quiz and earn an accredited certificate (with CMLE credits) to document your new competencies for supervisors and regulators.
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SuperNova Flow Cytometry is an independent educational provider with no affiliation, endorsement, sponsorship, and/or connection to Beckman Coulter, Inc. or Beckman Coulter, Inc.’s SUPERNOVA flow cytometry products.