See the Hidden: Discover More with FLIM

On Demand

Giulia Ossato, PhD

Senior Product Manager Confocal Advanced Microscopy, Leica Microsystems

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Ruslan Dmitriev, PhD

Assistant Professor, Ghent University

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Prof. Dr. Michelle Frei

Assistant Professor, ETH Zürich

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Mariano Gonzalez Pisfil

Staff Scientist, Ludwig-Maximilians-Universität München

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Jens Peter Gabriel

Advanced Workflow Specialist, Leica Microsystems

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Patrick McMillen, Ph.D.

Scientist, Tufts Center for Regenerative Biology and Medicine

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Dr. Boris Zarda

Advanced Workflow Manager, Leica Microsystems

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See how innovations in Fluorescence Lifetime Imaging Microscopy (FLIM) are driving discoveries in state-of-the-art applications, such as imaging oxygenation and cell metabolism in complex 3D models, harnessing epigenetic tools in live-cell microscopy, phasor analysis of multicolor imaging data, and more.

 

In this virtual workshop, you will learn:

  • The foundational principles and key applications of FLIM for delivering quantitative, molecular-level insights in biological research
  • Innovative approaches to enhance imaging resolution, distinguish multiple fluorescent signals, and analyze complex biological processes with greater clarity
  • How advanced imaging technologies like STELLARIS FALCON are redefining confocal microscopy

Join us for a virtual workshop focused on advancements in Fluorescence Lifetime Imaging Microscopy (FLIM) and the capabilities of the STELLARIS FALCON system by Leica Microsystems. The event will cover the principles and main applications of FLIM, emphasizing its role in providing quantitative molecular-level data.

Expert presentations and live showcases will explore the impact of these technologies on biomedical research and cellular imaging. Additionally, the workshop will feature discussions on recent developments, such as using red/near-infrared emitting cell staining oxygen-sensitive nanoparticles for measuring spheroid oxygenation and the engineering of HaloTag variants to modulate photophysical properties for live-cell multiplexing.

We will also explore multicolor FLIM approaches using phasor-based analysis to increase the number of distinguishable colors in laser scanning microscopy. This event will highlight how these cutting-edge technologies set new standards in confocal microscopy to enhance our understanding of complex biological processes.

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