CellEDIT - Engineered Cell Lines
Let CellEDIT accelerate your research by creating your custom engineered cell line, allowing you to focus on your discoveries.
We’ll handle the CRISPR editing of your cell line, so you can run your experiment faster and finish your project sooner.
Genome editing reagents are delivered into the cell through direct intranuclear injection without cargo-size limitations. By starting from injection of a defined number of reagents into single mammalian cells, we enable high editing precision and controllability. From knock-ins to knockouts, choose the CellEDIT service to outsource the generation of your engineered cells in 10 weeks.
Knockout
Engineered Cell Lines
Save time in the lab by powering your research with CellEDIT. Confidently streamline your drug discovery workflow and investigate gene function with effective CRISPR knockouts.
Multiplex
Editing of Cell Lines
At CellEDIT, we provide you with multiplexed cell lines in 10 weeks. The efficiency and gentleness of our vector-free editing through intra-nuclear delivery, makes it an ideal system to perform multiplex gene editing in one go.
Knockout Engineered Cell Lines
Access Knockout CRISPR Cell Lines without sacrificing time with CellEDIT's precision editing by direct intra-nuclear delivery of RNPs. In 10 weeks, we provide you with knockout monoclonal cell lines suited to your project needs.
Efficient on
Hard-to-transfect cells
Vector-free
direct intra-nuclear delivery
Minimized Off-Target
Immortalized Cell Lines
Learn how the CellEDIT workflow was used to generate 5 monoclonal Hprt knockouts in C2C12 cell line through direct intra-nuclear injection of only 51 cells.
Cancer Cell Lines
Discover how the CellEDIT workflow was used to produce 3 monoclonal HPRT1 knockouts in SK-MES-1 cell, a notoriously hard-to-transfect cell line.
Multiplex Gene Editing of Cell Lines
Within 10 weeks, we perform for you, the multiplex editing of your targeted genes. CellEDIT's vector-free intra-nuclear delivery ensures efficient and gentle gene editing, making it the perfect solution for multiplex gene editing in a single step.
Efficient on
Hard-to-transfect cells
Vector-free
direct intra-nuclear delivery
Minimized Off-Target
We know the challenges you're facing with your CRISPR projects and the time you've spent in the lab, repeating over and over your transfection experiment, adding months to research deadlines. CellEDIT’s optimized transfection workflow along with our direct control over the CRISPR RNPs injected volume, minimizes off-target effect and maximizes editing efficiencies.
About the CellEDIT Service
CellEDIT provides specialized cell line engineering services using patented technology that surpasses conventional methods in delivering CRISPR complexes directly to the nucleus, ensuring high-quality cell line engineering for your research. Guided by our experts, each project is tailored to your needs - from gRNA design and cell culture methods to gentle yet efficient delivery and personalized quality controls - preserving cell integrity throughout the whole process.
We know the challenges you're facing with your CRISPR projects and the time you've spent in the lab, repeating over and over your transfection experiment, adding months to research deadlines. CellEDIT’s optimized transfection workflow along with our direct control over the CRISPR RNPs injected volume, minimizes off-target effect and maximizes editing efficiencies.