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.
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.