RWD Lab Academy Webinar Session 3! Fluorescence Lifetime Photometry: Based on Intrinsic Fluorescence Lifetime, from Principle to 𝑰𝒏 𝒗𝒊𝒗𝒐 Application

Struggling with common challenges in Fluorescence Lifetime Photometry experiments?

1. How to avoid inter-group signal incomparability caused by differences in probe expression levels?
2. How to address the impact of excitation power fluctuations on signal stability?
3. During long-term recording, when signals decay due to photobleaching, how can true activity changes be distinguished?
4. How to enable direct comparison across brain regions and across animals?
5. How to obtain absolute quantitative values when intensity signals only reflect relative changes?

To address these challenges encountered in experiments, this RWD webinar will focus on the Fluorescence Lifetime Photometry System and comprehensively explain the basic concepts, core advantages, and typical application scenarios of fluorescence lifetime, helping you obtain stable experimental results and providing support for reliable quantitative analysis.

Webinar Topic: Fluorescence Lifetime Photometry: Based on Intrinsic Fluorescence Lifetime, from Principle to 𝐼𝑛 𝑣𝑖𝑣𝑜 Application

📅 Date: October 21, 2026
🕒 Time: 11:30 (EDT) | 10:30 (CDT) | 09:30 (MDT) | 08:30 (PDT) | 17:30 (CET) | 23:30 (BJT)
👩‍🔬 Speaker: Berry – RWD Solution Specialist

👉 : Free Register for Webinar Now>>

– Session Highlights
From principles to advantages, from scenarios to tools, helping you build a complete understanding, improve the efficiency of experimental design and data interpretation, and provide support for stable, reliable quantitative results.
1. What Is Fluorescence Lifetime?
2. Core Advantages Over Conventional Intensity-Based Fiber Photometry.
3. Application Scenarios of Fluorescence Lifetime Photometry.
4. Key Features of the RWD Fluorescence Lifetime Photometry System.

– Beyond Practical Skills: Discover the Powerful Solution Empowering Your Research

Fluorescence Lifetime Photometry System(FLiP) is based on Time-Correlated Single Photon Counting (TCSPC) technology with fiber photometry for real-time monitoring of fluorescence lifetime changes in the brain of freely moving animals, providing a stable and quantitative approach for in vivo studies of neurotransmitter release, protein-protein interactions, and protein conformational changes.

1. High Anti-Interference Capability: Fluorescence lifetime is an intrinsic physical property of fluorophores, independent of probe expression levels and excitation power fluctuations.
2. Long-Term Stability: Fluorescence lifetime is not affected by photobleaching, making it suitable for continuous recording over days or even longer.
3. Cross-Sample Comparison: Fluorescence lifetime enables direct comparison across different brain regions and animals.
4. Absolute Quantification: Fluorescence lifetime directly corresponds to the probe’s binding state, offering the potential for absolute quantification.

Interact during the webinar, and rewards such as needles and surgical instruments are waiting for you to take home!

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