Edit your desired target genes efficiently and accelerate therapeutic development with fast, cost-effective, and versatile workflows that make CRISPR gene editing technology accessible.
Targeted genome editing is a powerful tool for studying gene function, for modifying genomes to correct defective genes, and for introducing new functionality.
Learn how to successfully navigate translational research and make your progression from foundational research to clinical trials as smooth as possible.
Your Journey from Foundational Research to Manufacturing
Translational Research Focuses
Immunotherapy Development
Towards a Personalized Approach to Cancer Treatment
Immunotherapy has led to significant advances in our understanding and treatment of cancer. However, there is more work to be done. Explore the stages of cancer immunotherapy development and discover tools that assist you with your discovery at every stage.