Scientists wield nature’s power to optimize adeno-associated virus (AAV) production and maximize gene therapy safety.

An expert panel will present how synthetic biology accelerates the development of diagnostics, therapeutics, and the medicinal pipeline.

The Past, Present, and Future of Gene Therapy: How to Scale-up Successfully

A microfluidic device creates a single hole in each cell to allow efficient DNA entry without compromising viability.

A device for piercing individual holes in cell membranes allows vector-free DNA delivery while maintaining cell viability.

Recent developments in cell transfection and molecular delivery technologies

Levitating and manipulating objects using sound waves could help prevent contamination of materials.

Transfecting molecules into cells is as easy as one, two, squeeze.