Coursera Flash Sale
40% Off Coursera Plus for 3 Months!
Grab it
Explore cutting-edge cell therapy technologies in this 56-minute webinar presented by Daksha Patel, PhD and Fengmei Pi, PhD from GenScript. Discover how next-generation cell therapies are revolutionizing therapeutics by precisely engineering living cells for both ex vivo and in vivo applications using advanced CRISPR tools including Cas enzymes (Cas9, Cas12a), base and prime editors, and synthetic guide RNAs that enhance specificity, persistence, and potency beyond traditional methods. Learn about GenScript's comprehensive CRISPR toolkit and integrated RNA/LNP delivery platform that combines optimized RNA formats with targeted delivery strategies to accelerate CAR-T engineering, enhance in vivo delivery, and streamline the path from design to clinical application. Gain insights into precision genome editing through next-generation CRISPR Nuclease and OmniGuide RNA platforms designed for safe, efficient, and highly specific modifications. Understand advanced RNA formats including circRNA, StabiRNA, and novel capping strategies that extend RNA stability, enhance expression, and reduce immune activation. Examine how optimized RNA formats combined with lipid nanoparticles enhanced with ligand or antibody decoration enable efficient, targeted delivery to T cells and other tissues while streamlining workflows and improving therapeutic outcomes. Earn 1 PACE credit by registering as a Labroots member and completing the viewing requirements before the October 15, 2026 expiration date.
