New! Precision-Engineered Fibroblast KO Cells
Powered by our XDel CRISPR Technology, these cells deliver guaranteed knockouts for studying CNS disorders, fibrosis, and more.
Register for Our Upcoming Webinar!
Join our webinar to explore how Arctoris, EditCo and Brainxell are leveraging CRISPR-edited, iPSC-derived human microglia in automated, multiplexed assays to enhance disease modeling and drug discovery.
Introducing XDel CRISPR Technology
Introducing: The Future of Cell Engineering
At EditCo Bio, we're dedicated to making genome engineering easier, faster, and more reliable.
Building Functional, Reliable CRISPR-edited Primary Cells
Streamline your research with edited-to-order primary cells, including our new Knockout CD4+ & CD8+ T-cells.
Power Your Research with Knockout iPS Cells
Advance disease modeling, drug discovery, and regenerative medicine with EditCo's high-efficiency, precisely edited iPS cells.
Simplified CRISPR: From Design to Delivery
We make it easy for researchers to choose genes and yield and order in just a few clicks. Pick your genes and get started today.
We deliver optimized, multi-guide CRISPR kits and made-to-order edited cells.
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Explore CRISPR kits and engineered cell services.
Edited Immortalized Cells
Knockout Immortalized Cell Lines
CRISPR knockout cells streamline gene editing, providing ready-to-use cell lines and eliminating months of optimization.
Knock-in Immortalized Cell Lines
Receive precision edits for disease modeling and protein studies, bypassing the complexity of DIY CRISPR.

Edited iPS Cells
Knockout iPS Cell Lines
EditCo's CRISPR Knockout iPS Cells ensure industry-leading editing efficiency in iPS cells, without compromising cell quality. Get reliable gene knockout for critical gene function and disease linkage studies with the assurance of cell integrity.
Knock-in iPS Cell Lines
EditCo's advanced CRISPR knock-in edits in iPS cells unlock breakthrough potential in neuroscience and regenerative medicine. Our efficient automated process for high-quality reproducible iPS cell edits paves the way for your groundbreaking research and therapeutic development.

Edited Primary Cells
Knockout CD8+ and CD4+ T cells
Advance your immunology research with edited-to-order primary CD8+ and CD4+ T cells. Unparalleled editing accuracy and efficiency enable you to bypass the time and resources spent on optimization. EditCo's consistent and functional T cells ensure post-editing experimental reliability and robust downstream results.
Knockout Fibroblast Cells
Focus on the main experiment with made-to-order KO Fibroblast Cells. Whether you are studying autoimmunity, tumor micro-environments in cancer, wound healing, or other fibrotic diseases, EditCo has the solution to generate disease relevant models. EditCo’s XDel Technology enables high on-target editing efficiency in your disease models or target screens with Fibroblasts.

CRISPR Kits & Reagents
Gene Knockout Kits
Knockout any human or mouse protein-coding gene with our unique multi-guide RNA strategy. Three spatially coordinated modified SpCas9 sgRNAs induce fragment deletions, obtaining knockout rates greater than 80 percent, and it ships in as few as 5 days—the most reliable knockout strategy, guaranteed.
Arrayed CRISPR sgRNA Libraries
Achieve reliably high knockout efficiencies across your entire CRISPR screen for any human or mouse protein-coding gene. Identifying and validating your targets has never been faster and more reliable, with unparalleled quick delivery starting at 7 days and guaranteed editing efficiency.
Nucleases & Kit Add-ons
EditCo's highly efficient CRISPR kits simplify your science. Complete your CRISPR experiment with SpCas9 nuclease, transfection optimization kits, and add-on controls.

Leverage EditCo’s gene-editing expertise to support your research.


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Testimonials
As researchers studying SURF2's role in cancer resistance to chemotherapy, we investigated its depletion in U2OS and HepG2 cell lines. While siRNA yielded initial insights, we sought a more robust approach and partnered with EditCo to generate CRISPR knockout pools. They provided 100% homozygous deletions quickly, allowing us to validate results, isolate clones, and assess SURF2 knockout effects. This work led to our publication in Nature Communications (Tagnères et al.) and continues to drive our research. EditCo’s expertise and efficiency were instrumental, and we look forward to future collaborations.

EditCo has proven to be an invaluable partner in advancing our—and our client's—research. We highly recommend their gene editing services to any organization seeking a reliable, efficient, and skilled collaborator in the field of gene editing.

ATCC and EditCo’s strategic partnership brings together the gold standard in authenticated cell lines with EditCo’s leading CRISPR tools and gene editing services. This powerful alliance allows researchers to harness the highest-quality edited cells, accelerating their research with unparalleled speed, precision, reproducibility, and quality.

We chose EditCo's Arrayed CRISPR Library for our screening project after testing different reagents and finding that the multi-guide RNA design results in superior editing and knockout efficiency. This superior efficiency improves the sensitivity of our screen by enhancing our ability to detect phenotypes—in particular, weak phenotypes—resulting from knockouts.
At EditCo, our journey began within the pioneering gene-editing landscape of Synthego. Building on this expertise, we expanded into our own company, offering high-quality gene editing services, with a focus on precision cell engineering. With our experience as CRISPR leaders, our innovative editing platform, and the highest-quality gene editing products, we're here to propel our customers' scientific breakthroughs.
Partners in Innovation
When you partner with EditCo, you harness the transformative power of genome engineering for life science R&D and drive forward human health advancements. Through our Discovery Partners Ecosystem, we offer a unified platform from engineered cells to phenotypic data, streamlining the research process to accelerate drug discovery.






AI, CRISPR, and Automation in Oncology Drug Discovery
Learn how the team at Evariste has been using AI to accelerate drug discovery, along with the help of two powerful automated platforms: CRISPR editing through EditCo's XDel Cell Pools and assay development through Arctoris' Ulysses.
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Explore recent developments in genome engineering and multi-guide CRISPR kits.



