High Efficiency Cell Engineering Seminar - Hosted at the Catapult
Join us at the Catapult for an insightful seminar hosted by MaxCyte and Touchlight.
Tuesday 16th April 2024
12:00 PM - 2:00 PM
In-Person Event
Sycamore House
Leyden Road
Gunnels Wood Road
Stevenage
SG1 2BP
About the seminar
Join us on Tuesday 16th April for an in-person seminar hosted at the Catapult’s Sycamore House where we will discuss high efficiency non-viral cell engineering with MaxCyte electroporation and Touchlight’s MegaBulb DNA (mbDNATM), their novel circular single-stranded CRISPR knock-in template.
In this seminar you will find out how to rapidly drive your cell and gene therapy developmental efforts forward from research through to the clinic and commercialisation, safely and cost-effectively by leveraging MaxCyte’s flow electroporation® technology and Touchlight’s enzymatically manufactured DNA vectors.
Genome engineering of haematopoietic stem/progenitor cells (HSPCs) and T cells holds great promise for the treatment of diseases including cancer and genetic disorders. However, viral cell engineering has several limitations, such as high cost, lengthy manufacturing processes and the risk associated with viral integration into the host genome. Therefore, a non-viral genome editing approach has been gaining traction from basic to clinical research. MaxCyte’s clinical-scale flow electroporation efficiently delivers genome editing tools in the form of DNA, mRNA, RNP, and more recently Touchlight’s mbDNATM, into a wide variety of cells. mbDNA is a circular long single-stranded DNA (ssDNA), which shows low cellular toxicity and achieves high gene-length knock-in efficiencies, outperforming other non-viral technologies and rivalling viruses. mbDNA’s enzymatic manufacture, which leverages Touchlight’s established technologies and capabilities, addresses a major bottleneck for non-viral gene therapy development by facilitating access to long ssDNA as the optimal vectors for CRIPSR gene insertions. In this seminar, we will discuss high editing efficiency using MaxCyte electroporation to engineer clinically relevant cells with transposon-transposase or CRISPR-Cas9 platforms for knock-out or knock-in applications, while maintaining high cell viability.
Agenda:
12:00 – 12:30 pm: High efficiency cell engineering with the MaxCyte electroporation platform from concept to clinic, presented by Marianna Romito
12:30 – 1:00 pm: Non-viral cell engineering platform with MegaBulb DNA (mbDNATM) - a novel circular single-stranded CRISPR knock-in template, presented by Linda Meggiolaro
1:00 – 2:00 pm: Tour of the Catapult GMP training facility, coordinated by Ian Parnham
Please register to attend. Lunch will be provided for all attendees.
Speakers
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