CRISPR and Genome Editing – Multimedia

Speaking at the Advances in Drug Discovery & Development 2022 online symposium, Sterghios Moschos delivered his talk on targeted RNA therapeutics in the lung.

Download this infographic to discover tips and tricks on each stage of western blotting including sample preparation, electrophoresis, washing and blocking, and detection.

Speaking at the Advances in Drug Discovery & Development online symposium 2021, Agilent's own Peter Banks, Natalia Romero, and Brandon Lamarche delivered their talk on the analysis of cell division.

Speaking at The Landscape of Cancer Research 2021, Dr. Eric Kmiec, founder and director of the Gene Editing Institute, presented his talk on CRISPR-directed gene editing for solid tumors.

In less than 10 minutes, Professor Andrew Zydney covers: What are biopharmaceuticals? How do they differ from traditional small-molecule pharmaceuticals? How are they made? What factors might influence the high cost of biopharmaceuticals?

While CRISPR-edited cell lines can be beneficial for target identification, reagent validation, and biomarker discovery, generating high-quality cell lines can be fraught with difficulties and time-consuming and relies on several factors.

In this Teach Me in 10 episode, Lucy Lawrence is joined by Dr. Eric Wengert, postdoctoral fellow at The Children’s Hospital of Philadelphia to discuss gene therapies used to treat epilepsy.

Download this infographic to learn more about what cell and gene therapies are, how they are made, and advancements and future considerations in cell and gene therapy research.

Speaking at the Innovations in Disease Modeling online symposium 2022, Kevin holder, PhD, delivers his talk on Synthego's automated CRISPR platform for large-scale generation of cell models.

Gene therapy holds great promise for a wide range of diseases,
including cancers, cardiovascular diseases and thousands of rare
hereditary diseases caused by gene mutations.