Treating solid tumors with CAR-T cell therapy remains difficult, but with the advent of novel vector systems, such as transposons, coupled with tools like CRISPR/Cas9, researchers are making meaningful progress. This webinar examines how large-volume electroporation can support the reliable delivery of diverse clinically relevant cargo types, including DNA, mRNA, and CRISPR/Cas9 RNPs into large volumes of T cells.
Focusing on the next-generation 4D-Nucleofector® LV Unit PRO, the session will present case study examples showing how parameters optimized at small scale can be translated to clinical-scale manufacturing. Attendees will gain insight into how robust, GMP-aligned electroporation workflows enable efficient modification of up to one billion T cells, supporting knock-out, knock-in, and stable gene integration strategies for CAR-T development.
Attendees will learn:
Register to learn how the electroporation of clinically relevant cargos using transposon-based integration methods into large volumes of T cells holds significant promise for applications in the CGT space.
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