Detailed validation is key in successful drug development. Surface plasmon resonance (SPR) offers a label-free, direct-binding analysis that brings additional insights into drug kinetics compared to established functional assays.
SPR gives detailed information on affinity, complex half-life, thermodynamic constants and mode-of-action of potential candidates.
In this webinar, you’ll discover how SPR can be multiplexed and automated to enable high-throughput, data-rich drug candidate screening against multiple target proteins.
Watch this webinar to discover:
Cyrill Brunner, Ph.D., Senior Application Scientist, Bruker Switzerland, Fällanden, Switzerland
For Research Use Only. Not for use in clinical diagnostic procedures.