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New viral and non-viral platforms for T-cell engineering

Speaker

Abstract

Recent FDA approval of the first Chimeric Antigen Receptor T cell (CAR-T) therapy offers cancer patients more promise than ever for curative effects. However, many technical challenges in T cell gene delivery still remain in order for this therapy to become a standard of care practice. In this webinar, we will highlight the different viral and non-viral delivery approaches used in T cell engineering for cell and gene therapy applications including:

New solution for small-to-large scale serum-free, suspension lentiviral production – LV-MAX™ Lentiviral Production System

  • Platform development process using Design of Experiment (DOE) methodologies
  • High-throughput to large scale bioreactor protocols
  • Cost benefits of this system over current methods

Novel gene editing tools for primary T cells

  • New potent gene editing tools to increase knock-in and knock-out efficiency
  • Addressing non-viral delivery barriers through protocol optimization

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New viral and non-viral platforms for T-cell engineering


Specialty

Biotechnology

Medicine

Gene Editing

Crispr-Cas9

Cell Culture

Cancer Research

Stem Cell Technologies

Neuroscience

Gene Expression

Developmental Biology

Cell Signaling / Transduction

Cancer Therapeutics

Brain

Assay Development

Oncology

Geography

Asia50%

North America33%

Europe17%

Registration Source

Website Visitors100%

Job Title

Research Scientist40%

Clinical Laboratory Scientist20%

Marketing/Sales20%

Lab Management20%

Organization

Clinical Laboratory17%

Biotech Company17%

Medical School17%

Other17%


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