Newsletter | October 1, 2025

10.01.25 -- Inside CRISPR-GPT, An AI-Driven Multi-Agent System

SPONSOR

Webinar: Development of an Off-the-Shelf γδ T-Cell Platform for Allogenic Cell Therapies

Unlock the future of cell therapy with Miltenyi! Join our webinar to explore how γδ T cells are driving next-generation, off-the-shelf allogeneic therapies. Discover their unique advantages, learn engineering strategies to overcome immunological hurdles, and see a real-world case study of a successful therapeutic candidate. Don’t miss this chance to gain insights into the future of immuno-oncology. Click here to learn more.

FOCUS ON TRANSLATIONAL RESEARCH

Cell & Gene Podcast: Inside CRISPR-GPT With Yuanhao Qu

In this episode, Host Erin Harris talks to Stanford School of Medicine Ph.D. student, Yuanhao Qu, about his work developing CRISPR-GPT, an AI-driven multi-agent system designed to automate genetic experimental design and data analysis, making CRISPR experiments more efficient and accessible, even for non-experts.

Standardize Flow Cytometry Data With Easy Assay Transfer Across Sites

Seamlessly transfer and standardize flow cytometry assays across multiple instruments and global sites. Learn how modern flow cytometers can simplify this process and improve data consistency.

High Efficiency Cell Engineering: Best-In-Class Electroporation

Maintaining high cell viability and recovery is crucial for the success of gene editing, cell-based assays, and the production of proteins and viruses. Explore how non-viral gene-editing platforms can be used.

Guidelines For Comparing SYBR Green Master Mixes

A straightforward protocol for comparing qPCR master mixes is key to ensuring reliable results. See how to evaluate specificity, PCR efficiency, and precision to ensure accurate gene expression analysis.

SPONSOR

Webinar: Evolving Gene Editing for Rare Disease Drug Development

Danaher is partnering with leading academic and clinical research institutes focused on the development of a novel platform approach to gene editing aimed at accelerating the delivery of therapies and creating economies of scale to treat ultra-orphan conditions. We will explore how to create scalable models for efficient manufacturing and broader patient access and formulate regulatory and clinical strategies to address rare disease challenges. Learn more.

TRANSLATIONAL RESEARCH SOLUTIONS

Validated Non-Proprietary Assay (NPA) List - Aliri Bioanalysis

A Platform For Measuring Multiple Critical Bioprocess Parameters - Repligen – PAT

EVENTS

Advancing the Future of Cell & Gene Therapy

This 11-12 November, Cell 2025 unites 1,000+ leading experts across the CGT value chain to solve key challenges, from scalable bioprocessing and regulatory hurdles to accelerating development timelines.

 

Gain practical strategies across cell culture, therapy development, and CGT manufacturing, and hear from world-renowned leaders Bobby Gaspar (CEO, Orchard Therapeutics), Christof Von Kalle, (Director & BIH Chair, Research Clinic Luxemburg), and Dame Molly Stevens (University of Oxford). Register Now

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