Transgenic Model Creation Services
Charles River works with global customers on unique transgenic models to deliver study-ready cohorts to meet research needs. Our dedicated project management team, scientists, and animal care staff are always available to offer guidance, develop work plans, and help overcome any challenges.
Transgenic Mouse and Rat Model Creation
Learn more about CRISPR/Cas9* for genome editing, animal model creation, gene therapy, and modelling human disease by watching our webinar series. View Series
Global Service Offerings
Through partnerships with genomics industry leaders, our combined expertise provides an optimum environment for generating, characterizing, preserving, and distributing your transgenic lines.
CRISPR/Cas9 Genome Editing in Mice and Rats
Create and maintain the right model for studies using CRISPR/Cas9. This technology is used to knockout or modify DNA in animal models to study phenotypes and develop new treatments.
Custom RNAi Mouse Models
RNAi-mediated gene silencing makes complex genetic modifications easier to achieve more quickly and efficiently than traditional knockout technologies. The estimated timeline from project initiation to the generation of ES cell-derived RNAi mice is an estimated 24 – 30 weeks.
ES Cell Mutagenesis in Mice
With ES cell technology, our microinjection experts inject custom ES cells directly into blastocysts, effectively bringing your in vitro research models to life.
- Knockin/Knockout Mice
Bridge the gap between your in vitro and in vivo mouse models by using ES cell, DNA, and CRISPR microinjections.
Random DNA Transgenesis in Mice
The DNA vector is injected directly into the pronuclei of zygotes, bringing your customer in vitro models to life with founders available in three to four months.