PC-3 Cell Engineering with CellEDIT
— Take control of PC-3 engineering with the combination of gentle vector free delivery method and CRISPR technology.

The Challenges of PC-3 Cell Engineering

Struggling with your CRISPR experiments?
Standard methods like lipofection or electroporation can damage cells and are less effective on challenging cell types like PC-3.
Alternatives like viral transduction come with additional risks of uncontrolled integration and may trigger an immune response.
If your current approach isn't working, it may be time to try something gentler and more effective.
Gene Engineering with CellEDIT
Precision CRISPR Cell Line Engineering with FluidFM: Innovative Vector-Free Methods for Transfecting Challenging Cell Types.
Direct intranuclear delivery
FluidFM-based Nanosyringes inject genome editing reagents directly into the nucleus of a single cell.
Vector-Free Technology
No viral vectors, ensuring precise and controlled genome editing.
Gentle & Effective
Force-controlled injection enables genome editing in hard-to-transect and sensitive mammalian cell lines with minimal cell perturbation.
Seamless Cell Line Editing:
From Order to Delivery in 5 Simple Steps
Our streamlined five-step process ensures precision, speed, and reliability—from your initial request to the delivery of your customized cell line. We handle every detail so you can focus on your research.
Here's how it works:
1. Project Overview
Week 1
- Editing Strategy design report
- gRna Design
2. Onboarding Email
Week 2-5
- Thawing
- Mycoplasma test
- Contamination test
3. CellEDIT Workflow
Week 5-9
- Status update
- Injection
- Singulation
- Outgrowth
4. Clone Analysis
Week 10
- Genotyping
- Mycoplasma test
- Cryopreservation
5. Report & Shipment
Week 10
- 2 edited and 2 wild type clones Shipped
*Week 1 starts when the cell arrives at Cytosurge. The exact project timeline depends on the doubling time of the clones.
Ready To Get Started
Schedule a free consultation to learn more about our CellEDIT offer.
Our experts will help design a solution tailored to your research goals. No commitment—just transformative results.
CellEDIT Quoter
Use our calculator to configure your custom cell line and plan your gene editing project with confidence
Book a Consultation
Schedule a consultation today and learn how our pioneering approach can optimize your CRISPR workflow
Real Results from Leading Scientists:
Discover How Our Technology is Transforming Research.
CellEDIT Technology
Precision CRISPR Cell Line Engineering with FluidFM:
Innovative Vector-Free Methods for Transfecting Challenging Cell Types
At Cytosurge, we advance cell engineering with our unique single-cell technology. Our vector-free, gentle intra-nuclear injection speeds up research while ensuring accuracy and control.

Direct Nuclear Delivery
FluidFM-based nano-syringes inject genome editing reagents directly into the nucleus of a single cell.

Vector-Free Editing
No viral vectors, ensuring precise and controlled genome editing.

Minimized Off-Target
Force-controlled injection enables genome editing in hard-to-transect and sensitive mammalian cell lines without disruption.
Unlock new possibilities in cell research with precise and efficient gene editing
Achieve reliable, high-quality genetic edits with our CellEDIT service. Our gentle, intra-nuclear delivery ensures accurate modifications, even in hard-to-transfect cells. We work with a range of cell lines, including U20S, CHO, HeLa, MCF-7, C2C12, HEK293, MDA-MB-231, A549, and KPC. Streamline your research with our expertise.