Gene-Editing Services

Runtogen's customized gene editing services leverage the precision of CRISPR/Cas9 technology to perform a variety of genetic modifications, including SNP replacement, gene knock-in, and DNA knock-out. We specialize in editing tumor cell lines, other cell models and microorganisms to accelerate your research and therapeutic development.

Knockout Cell Line Service

Frameshift, stop codon, fragment deletion
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Knockin Cell Line Service

Single nucleotide mutation, small fragment replacement
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Overexpression Cell Line Service

Reporters, exon duplication, overexpression, safe harbor sites etc.
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Knockdown Cell Line Service

Gene silencing by RNA Interference (RNAi)
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Microorganisms Gene Editing Service

Knockout, Overexpression, Point mutation, Knockin services in Escherichia coli, Salmonella and Pseudomonas aeruginosa.
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Why Work With Runtogen

Expert Team

Our team consists of experienced scientists and industry experts dedicated to delivering the highest-quality gene editing and cell line development services.

Precision & Efficiency

We employ the latest technologies to ensure precise, reproducible results, saving you time and resources in your experiments.

Customer-Centered Approach

We collaborate closely with clients to tailor our services to meet their specific needs, ensuring optimal outcomes for each project.

Fast Turnaround

We understand the importance of time in research. Runtogen is committed to providing quick, reliable services with the fastest turnaround times possible.

Frequently Asked Questions (FAQs)

  • Knockout, Knockin, Knockdown, Overexpression, Point Mutation In Cell Lines
  • Gene-editing Services in Microorganisms

Cell Lines to be edited: Runtogen provides a wide collection of Tumor cell lines and othe cell lines for the customers to choose from. 

The Gene Information(ID or Sequence)

It takes 1-5 months depending on the recovery of the cell lines, the proliferation rate and transfection efficiency of the cells, and validation assays requested by the customer. Speedy turnaround as fast as 4 weeks! 

Exclusive innovative technique, Gene-editing efficiency improved by 10-20 times. With MagCRISPR™, Runtogen has successfully modified 8,000+ genes from more than 200 cell lines with our exclusive innovation MagCRISPR™ technology.

Standard deliverables:

  • 2 frozen vials of each clone with sequence verification
  • Parental cell line
  • Functional verification for Cas9 stable and reporter cell line projects
  • Mycoplasma testing
  • Sterility testing
  • Summary project report