CRISPR Custom Knockout Cell Line Generation Service
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ASC provides comprehensive custom service to generate gene knockout cell lines using its successful CRISPR/Cas9 cell line model generation platform. With >1300 unique cell line models generated to-date and in >200 distinct mammalian cell lines, we can generate a cell line model to your specifications, in as little as 2 months.
- Frameshift mutation, fragment excision, stop cassette insertion, double gene knockout
- Homozygous/ heterozygous knockout clones
- Variety of cell lines: cancer, hard-to-transfect, most mammalian species
- gRNA design, construction, and validation
- Donor DNA construction (if needed)
- Cell line validation, transfection and optimization
- Screening for single cell clones and clone confirmation
- Cell expansion and cryopreservation
- Two homozygous clones with correct gene mutation for the modified line; two vials of each clone; 1 x 10^6 cells/vial.
- Milestone update/report; final report with detailed description of each procedure, including targeting vector design, construction and validation, transfection condition, genotyping strategy, and results.
Timeline: 3-4 months
- Disease modeling for immuno-oncology, pharmacogenomic studies
- Drug discovery and drug efficacy and toxicity screening; drug combination studies
- Antibody validation
- Deriving diagnostic reference standards and materials
- Recombinant protein production in CHO cells
- Generation of TARGATT™ master cell lines by inserting an attP "docking site" for site-specific gene knock-in