StemEdit combines REPROCELL’s clinically aligned StemRNA™ iPSC technology with AI-designed OpenCRISPR-1™ (OC-1) editing tools to enable precise, reproducible, and scalable genome engineering workflows without licensing restrictions.
Key Benefits
✓ License-free
✓ Precise Genomic Integration
✓ Translationally Focused
✓High on-target editing efficiency
OC-1 , licensed from Profluent Bio, forms the foundation of REPROCELL's StemEdit platform. REPROCELL has expanded the platform beyond the core nuclease by developing integrated gene editing products, engineered cell lines, and custom genome engineering services, providing a comprehensive, license-free solution for stem cell research and translational development.
*StemEdit is provided without licensing requirements for the editing platform. Customers remain responsible for ensuring freedom to operate for their specific therapeutic targets and intended commercial applications.
Find the right solution for your research or
cell therapy development program
StemEdit Gene Editing Service
Clinical & Research Projects
Custom gene editing services for iPSCs and mammalian cells including knockouts, knock-ins, multiplex editing, and hypoimmune engineering.
Landing Pad Technology
Part of StemEdit Service
Precise insertion of therapeutic genes into engineered cells. Reuse an established landing pad to efficiently add or exchange genes, saving time and reducing lab costs.
StemEdit
B2M & CIITA KO Lines
Research Use
Ready-to-use, hypoimmune iPSC and iMSC lines with B2M and CIITA knockouts. Ideal for allogeneic cell therapy research and off-the-shelf applications.
StemEdit
OC-1 Protein
Ready for Your Laboratory
AI-designed OpenCRISPR-1 (OC-1) protein delivers strong editing activity, SpCas9-like on-target performance, and reduced off-target effects.
StemEdit Platform Overview
Gene Editing Services
StemEdit Gene Editing Service is REPROCELL’s AI-designed gene editing platform for advanced stem cell engineering, supporting both research and translational cell therapy applications. Combining StemRNA™ Clinical iPSC Seed Clones with OpenCRISPR-1 (OC-1) technology from Profluent Bio, StemEdit enables high-efficiency genome editing with reduced off-target effects in mammalian cells, including iPSCs, HEK, CHO, and primary cells.
StemEdit OC-1 Protein
REPROCELL also offers StemEdit OC-1 Protein for high-efficiency gene editing directly in your lab. Designed using AI-trained protein language models, OC-1 delivers strong editing activity, SpCas9-like on-target performance, and compatibility with base editing workflows for precise genome engineering applications.
Advanced Cell Engineering
StemEdit supports custom gene editing services, hypoimmune cell engineering, and Landing Pad Technology, a modular platform for precise, reproducible insertion or exchange of therapeutic genes. REPROCELL also offers ready-to-use StemEdit B2M & CIITA knockout hypoimmune iPSCs and iPSC-derived mesenchymal stem cells (iMSCs) designed for allogeneic cell therapy and regenerative medicine research.
Supported Applications
-
Hypoimmune cell engineering
-
B2M and CIITA knockout generation
-
Custom iPSC engineering
-
Landing Pad integration
-
Therapeutic transgene insertion
-
Disease model development
-
Regenerative medicine research
-
Allogeneic cell therapy workflows
-
Stem cell engineering
- Translational genome editing
Related Pages
Related Blogs & Webinars
Contact our experts
Discover More
- GMP iPSC Production Service
- GMP iMSC & MSC Production Service
- iPSC-Derived Exosome Production Service
- GMP iPSC/iMSC MCB Manufacturing – REPROCELL USA
- GMP iPSC/MSC MCB Manufacturing – Histocell (Europe Partner Overview)
- REPROCELL Japan GMP Manufacturing Facility
- For clinical use: Ready-to-use GMP MSCs
Resources
- FAQ: Clinical iPSCs
- FAQ: Clinical MSCs
- FAQ: iPSC-Derived Exosomes
- Making iPSC-Derived Therapeutics a Clinical Reality – our external article in the European Biopharmaceutical Review.
On the REPROCELL blog
Latest in Gene Editing
AI-Designed CRISPR Enables Hypoimmune iPSC Engineering for Off-the-Shelf Cell Therapy
REPROCELL's StemEdit platform enables the creation of hypoimmune iPSCs for scalable off-the-shelf cell therapies, reducing immune rejection and enhancing patient access.
04 June 2026
What Are Off-Target Effects in Cellular Gene Editing? Risks, Detection, and Solutions
Explore off-target effects in gene editing, from CRISPR risks and AI-driven detection to genomic safety in iPSC therapies.
20 May 2026
5 Hard Truths About Bringing Stem Cell Therapies to the Clinic
Discover the essential truths behind developing clinical-grade stem cell therapies and learn how to navigate the complexities of GMP manufacturing successfully.
30 March 2026




