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Runtogen

Knockout Cell Line Service

Knockout Cell Line Service

Knockout Cell Line Service

CRISPR/Cas9-based knockout cell lines delivered in 4–12 weeks. Fully validated and publication-ready.

Runtogen offers fast, reliable, and fully validated knockout (KO) cell line services using our unique gene-editing platform including CRISPR/Cas9. Whether you need a single-gene knockout for basic research or multiple knockouts for drug screening, our customized solutions are designed to meet your exact needs.

 

 

Crispr genome editing is most direct and fastest approach to achieve the knockout of a specific gene or double genes. Runtogen’s CRISPR Gene Knockout Cell Line Service provides end-to-end support for generating custom knockout cell lines using advanced CRISPR Cas9 gene-editing technologies. Researchers can specify the gene(s) of interest, the cell type, and the level of validation required. Our expert team utilizes CRISPR Cas9 technology to tailor genome editing to your specific requirements. 

Type of Gene Editing

CRISPR Cas9

CRISPR Design

Synthetic Modified sgRNA (Standard)

Types of Cells
  • * Tumor cell lines
  • * Stem cells
  • * IPS cells
  • * Non-stem cell lines
Available Edits

Frameshift, stop codon, fragment deletion; Single, Double, or Triple Knockout

Our Knockout Cell Line Workflow:

 

Knockout Cell Line Service

Why Choose Us?

Ready to Start Your Knockout Project?

Contact us today to discuss your target gene, host cell line and get a free consultation within 24 hours.

Knockout Cell Line Case Study: Human GAL Knockout model in HCT116 Cell Line Service

 

GAL locus in human colon cancer cell line, HCT116, was knocked-out by creating indels in exon 3, as shown in the targeting strategy.


PCR Identification for positive clones

 

 

Individual clones were Sanger sequenced to select for homozygous knock-out indels of GAL at exon 3. Sanger sequencing data. del 251 bp (E3 is completely deleted)



KO CELL lINE Service Brochure (PDF)

FAQ

A knockout (KO) cell line is a cell line where a specific gene has been deliberately “knocked out” or deactivated using gene-editing technologies like CRISPR/Cas9. This allows researchers to study the effects of gene loss on cell function, which can be essential for drug development, disease research, and understanding cellular processes.

We create knockout cell lines using advanced CRISPR/Cas9 technology. This technique allows precise editing of the target gene by introducing a double-strand break in the DNA, which is then repaired incorrectly, resulting in gene disruption. We also provide alternative methods such as RNA interference or gene silencing for certain applications.

We work with a wide range of cell types, including tumor cell lines (like HEK293, HeLa, etc.), primary cells, and stem cells. The choice of cell line depends on your research goals and the specific requirements for gene knockout.

The typical timeline for generating a knockout cell line is between 4-12 weeks, depending on the complexity of the project and the cell type being used. This includes the design, transfection, screening, and validation of the knockout.

Our Knockout Cell Line service includes:

  • *Gene design and CRISPR guide RNA synthesis

  • *Transfection or viral transduction of cells

  • *Screening for successful gene knockout

  • *Clonal isolation and expansion of knockout cells

  • *Verification via PCR, Western blotting, or other assays

  • *Custom support for specific needs, including cell culture optimization

We use multiple verification methods to ensure the gene knockout is successful. These may include:Sanger sequencing, Western blot, and functional assays included

Yes, dual knockout and conditional KO (Cre-lox) are available upon request.

Our success rate for generating functional knockout cell lines is high, typically around 95-100%. Success depends on factors such as gene size, target cell type, and the specific experimental conditions. We will work closely with you to optimize the process and achieve the best possible results.

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