Gene therapy using adeno-associated virus (AAV) vectors is a rapidly emerging field, with many treatments in development and two recent FDA approvals. In this webinar, we will discuss the development of fast anion exchange chromatography methods for the analysis of full and empty AAV capsids. Baseline separation of full and empty capsids of several different serotypes using either salt gradient or pH gradient methods will be presented.
Key Learning Objectives:
- Learn about AAV vectors growth in biotherapeutics
- Learn about ways to analyze adeno-associated virus vectors
- See method development using AEX method analyzing both full and empty AAV capsids
Who Should Attend:
- Research Scientists
- Application Scientists from Biopharma companies working on or interested in gene therapy
- PhD students in any field of biotherapeutic drug development
- Scientists looking to advance knowledge of gene therapy
Register here
United States
