This educational webinar will cover the practical aspects of using Adeno-Associated Viruses (AAV) and lentiviruses to deliver and express Your Favourite Gene (YFG) in vivo for both basic research and pre-clinical studies of gene therapy treatments.

With expertise in translational neuroscience, Professor Stephanie Schorge, Dr Ahad Rahim and Dr Giulia Massaro, will highlight tips and tricks to help any researcher use viral delivery for basic and translational neuroscience. This will include:

How to design a viral vector and which capsid to use
What is needed to make viral particles
How many are needed for different studies
What resources are available for help, including the new UCL GeneTxNeuro Facility based at the UCL School of Pharmacy

GeneTxNeuro is a facility that gives all UCL researchers access to the equipment and expertise needed to make AAV and lentis for research and preclinical work.

The webinar will highlight the services and benefits offered by the facility, including:

Providing expertise and support for new and established researchers wishing to design, synthesis and use these tools.
Extra support for researchers not experienced with viral work from a dedicated research fellow with extensive expertise who can help advise on aspects from design of the expression cassette to injection of the vector.
Information sharing for gene therapy users across UCL to share best practice and innovations to keep UCL at the front of this field.

Who should attend?

Basic and translational researchers from across UCL at any career stage (PhD students to PIs) with an interest in gene therapy and learning more about what research questions they may address with the tools and services offered by the facility.

Expand your experimental toolkit: Viral delivery tips for all researchers