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Viral-Vector Solutions: Enhancing the Development of Cell & Gene Therapy Treatments

 
On-Demand Webinar
 
CANVA_Oncology-Week_Webinar2_Laptop (1)

About the workshop

At the forefront of therapeutic delivery, viral vectors hold immense promise for precision medicine in oncology. While lentivirus plays a critical role in the emergence of cell therapies through genetic modifications, such as CAR-T therapy, adeno-associated virus (AAV) vectors are emerging in cancer gene therapy. Explore the development process of viral delivery systems for oncology therapeutics, including complete workflow solutions, from synthesis through production and confirmation, to tackle challenges and optimize downstream success.

 

What you'll learn about

  • The development of the viral-vector pipeline, including synthesis, packaging, and characterization of the viral-vector product
  • How recent solutions can evaluate post-treatment samples for expression confirmation and analyze samples for unwanted or off-target insertions

 

Unable to attend live? Register today and we’ll send the recording to watch at your convenience.

About the presenter

ELouie

Elizabeth (Liz) Louie, Ph.D.

Manager​, Technical Applications, Azenta Life Sciences

Dr. Elizabeth Louie earned her Ph.D. in molecular and cellular pharmacology from Stony Brook University. She joined Azenta in 2011, overseeing gene synthesis and molecular genetics projects while supporting the Project Management team with customer-facing project design and execution. Later, she led the expansion and management of molecular biology and oligo synthesis operations at the Azenta genomics facility in Boston, MA. Currently, Dr. Louie provides consultative and project design support for researchers and investigators, focusing on genomics, transcriptomics, and proteomics solutions. Her expertise includes next generation sequencing (NGS), DNA and RNA synthesis, genotyping methods, and cell and gene editing workflows.

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