A complete cell engineering solution from start to discovery

To help researchers in their quest to understand how the genome influences phenotype, we’ve developed the only complete toolset comprising trusted solutions for every step in the cell engineering workflow. Our collection of optimized, validated technology systems are designed to work together to eliminate the trial-and-error phase and help you get answers faster and with less effort.  Every lab is unique, so we offer a range of genome editing solutions to cater to your needs. Whether you want results fast, seek full control over every step in designing your gene edit, or need help with engineering cells to your specific needs, we have solutions that fit.

Which technology?   Request Genome Editing eBook  

Featured technologies

Rapid and efficient editing with multiplexing capabilities.

Precise and flexible editing; targeting to any gene in any cell, with all-around freedom.

Quickly design optimal CRISPR gRNAs with minimal off-target effects. 

Largest collection of ready-to-go CRISPR cell lines.

Optimized products & protocols for optimal CRISPR-Cas9 delivery.

Essential tools for monitoring the efficiency of your genome editing experiments.

Featured genome editing applications


Design to analysis in just four days! It doesn't get easier than this. The ultimate 4-day workflow using CRISPR protein.


Modify and study gene and protein expression, and explore disease and differentiation pathways, using a variety of gene delivery techniques.


We now offer both off-the-shelf engineered cell lines and custom design and engineering services to deliver the cell lines you need with high quality and service.

Featured videos

The Power of CRISPR Editing

Discover CRISPR Engineered Cell Models

Need assistance with CRISPR gRNA design?

Our CRISPR Search & Design tool allows you to search our database of >600,000 predesigned CRISPR gRNAs in human and mouse genes or analyze your sequence of interest for de novo gRNA designs using our proprietary algorithms. Up to 25 gRNA sequences per gene are provided with recommendations based on potential off-target effects for each CRISPR sequence.

Start designing today ›