Join AbbVie scientists Shitalben Patel and Jami R. Erickson as they showcase their innovative advancements, transforming CETSA® into a high-throughput flow-based platform and introducing new whole blood formats to elevate drug discovery.In this webinar, you’ll learn about flow-based CETSA, a powerful, high-throughput technique that enables single-cell target engagement analysis without cell lysis. Designed for screening of large compound libraries, this method overcomes traditional limitations like low throughput and high cell input. You will also hear how the method is being integrated into real-world SAR funnels to accelerate hit generation.
In the second half of the webinar, you will learn about novel Alpha and MSD CETSA formats for whole blood, using RIPK1 as a proof-of-concept. These assays require <100 μL of blood, eliminate PBMC isolation, and deliver clinically relevant, reproducible readouts—bringing true target engagement measurement closer to patient-derived samples.
Don’t miss this opportunity to explore how these CETSA innovations can transform your approach to drug discovery—from high-throughput screening to clinical translation.
Key Topics:
- High-Throughput CETSA Innovation: Learn about the flow-based adaptation of CETSA, enabling rapid, large-scale compound screening using 384-well plates.
- Flow Cytometry-Based Methodology: Discover how this technique detects thermostabilized proteins without cell lysis, allowing detailed single-cell analysis.
- Application in Drug Discovery: See how flow-based CETSA integrates into SAR funnels, accelerating hit generation for endogenous targets in native cells.
- Whole Blood CETSA Development: Explore two novel formats—Alpha CETSA and MSD CETSA—that use <100 μL blood and eliminate PBMC isolation.
- Clinical Relevance: These blood-based assays enable direct, scalable target engagement readouts and support asynchronous, centralized clinical workflows
- Translational Potential: Together, these innovations bridge preclinical research and clinical application, streamlining drug development in native biological systems.
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