Resource Center
Explore Resource Types
We have housed the technical documents (SDS, COAs, Manuals and more) in a dedicated section.
Explore all All Resources
Filters
Select resource types (1)
Select products & services
Select solutions (1)
Active Filters (2)
Clear All
1 - 12 of 18 Results
Sort by:
Best Match
Whitepaper
Accelerating immuno-oncology therapeutic development: choosing the best preclinical model
Selecting the appropriate preclinical model for immuno-oncology therapeutic development.
Whitepaper
Precise cell engineering
Explore the advanced capabilities of the Pin-point™ base editing platform for multiplex gene editing and its application in T cells and iPSCs. Discover how CITE-Seq enables deeper insights into single-cell phenotyping and cell therapy development.
Whitepaper
Optimizing AAV manufacturing: a scalable harvest protocol
As demand for recombinant AAV (rAAV) vectors continues to rise, scalable and efficient manufacturing processes are essential for advancing gene therapy.
Whitepaper
ImmuSignature™ MLR: Rapid high-throughput assessment of therapeutic immunogenicity
This white paper describes how a rapid immunogenicity assessment screening can provide invaluable support for IND applications.
Whitepaper
Assessing the epigenetics of T cell exhaustion using CRISPR screens
Explore the epigenetics of T cell exhaustion and practical techniques to assess immune cell epigenetic regulators using CRISPR screens.
Whitepaper
Base editing and stem-cell based therapies
This white paper explores how base editing is advancing iPSCs in the fields of basic science, regenerative medicine and immunotherapy.
Whitepaper
Addressing the challenges in solid tumor therapy with base editing
Read this white paper to learn about how base editing is helping to address key challenges in immunotherapies for solid tumors.
Whitepaper
Finding the right technology for your genome engineering project
Learn about how to select the right technology for your genome engineering project in this white paper.
Whitepaper
Generating a clonal HAP1LIG4(-) Cas9(+) cell line – an expert interview
An interview with Dr. Gerety, the Sanger Institute on generating a new HAP1 cell line and how it can help advance scientific discovery.
Whitepaper
CRISPR-derived base editing technology: The what, the how, and the why
This white paper provides a comprehensive guide to base editing, including what it is, how it works and applications.
Whitepaper
AAV vectors: Pursuing a one-time therapy for ocular diseases
Explore the latest advancements in gene therapy and its transformative impact on ocular health.
Whitepaper
Innovative approaches for advancing genetic payload development
Discover the future of gene therapy in our white paper 'Innovative approaches for advancing genetic payload development.' Learn about the challenges and breakthroughs in gene editing, offering a glimpse into the evolving landscape of genetic medicine.
Looking for technical documents?
Find the technical documents you need, ASAP, in our easy-to-search library.