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Power What Matters to You in Immunology Research

Join us for an exclusive educational event designed to help you streamline panel design, extract deeper insights from every sample, and harness the full power of spectral flow cytometry. Through expert insights and real-world applications, you’ll learn how to do more with less—capturing richer, more meaningful data with greater efficiency.

 

 

Where

 

Northwestern University
Simpson Querry Auditorium, SQBRC 1-230

303 E Superior St

Chicago, IL 60611

 

Parking: Several parking lots and metered parking around the venue

 

 

Agenda
 

9:00 - 10:00 amRegistration
10:00am -11:30 am

Identify & Design: The Power of Choice


Length: 60 minutes + Q&A


Discover how to select the best fluorochromes for your experiments while understanding their impact on panel performance. This module combines insights into key attributes such as brightness, spillover, stability, and background, with a structured approach for choosing reagents that aim to deliver optimal resolution of cell populations in both small and large panels.


In this module, we’ll cover:

  • Fluorochrome properties that may impact panel performance, with examples.
  • How to use brightness and spillover when selecting fluorochromes.
  • An approach compatible with panels for conventional and spectral flow cytometry.
11:30am -12:30 pm Collaborative Lunch and Conversation
12:30pm – 1:45 pm

Discover & Reveal: The Power of Dimensions


Length: 60 minutes + Q&A


Explore how spectral flow cytometry combined with spatial information at the single-cell level expands the possibilities for biological insights with sub-cellular resolution. This module integrates the principles of fluorochrome selection for well-performing panels with the added dimensions from signal-derived imaging parameters to uncover hidden biology.


In this module, we’ll cover:

  • How the future has changed with real-time imaging, spectral flow cytometry.
  • Revealing what was missed with added dimensions from imaging parameters.
  • An example of a T-bet translocation assay using 14 colors with imaging and spectral flow cytometry and 9 multiplexed samples (fluorescent cell barcoding).
1:45pm – 2:30 pm Q&A

 

 

 

 

 

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