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Runtogen

Knockout Cell Line Service

Knockout Cell Line Service

CRISPR knockout Cell Line Service

Runtogen’s MagCRISPR™ KO Cell Line Service is a specialized offering designed to help researchers create cell lines with specific genes knocked out, tailored to their experimental needs. CRISPR Knockout Cell Line service is ideal for studying gene function, disease mechanisms, drug target validation, and more.

 

 

CRISPR gene 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. Whether you require permanent knock-out or conditional knock-out, we have you covered.

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

Knockout Cell Line Service Working Flowchart:

Why Choose Runtogen’s Knockout Cell Line Service?

*State-of-the-Art Genome Editing

We utilize advanced genome editing technologies, including CRISPR/Cas9, TALENs, and ZFNs, to achieve precise and efficient gene knockouts with high specificity.

*Comprehensive Validation

Our knockout cell lines undergo rigorous validation at the DNA, RNA, and protein levels, ensuring reproducible and reliable experimental outcomes.

*Customized Solutions

We tailor the knockout process to accommodate various cell lines and research objectives, providing flexible solutions for diverse experimental needs.

*Expert Scientific Support

Our experienced team offers comprehensive guidance, assisting with experimental design, troubleshooting, and technical support throughout your project.

Deliverables

 

  • *Biweekly project updates for real-time progress tracking
  • *Homozygous and heterozygous cell clones tailored to your requirements
  • *Control-transfected cell pools for comparative analysis
  • *Synthetic sgRNA sequences used in genome editing
  • *Primer sequences for PCR and Sanger sequencing validation
  • *Sanger sequencing analysis reports to confirm successful gene knockout
  • *Comprehensive quality control (QC) report ensuring the integrity and accuracy of results

 

 

Contact us today to discuss your knockout cell line project, and let us help you advance your research with custom-engineered cell lines tailored to your specific needs. Whether you are studying gene function, disease mechanisms, or therapeutic strategies, our knockout cell line service will help you achieve your scientific goals.

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)



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

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