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Cas9 Stable Cell Line - CHO-K1

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RO01172 Host Cell :   CHO-K1

Size :   >1x106 cells/vial Validation :   T7 Endonuclease I assay

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Cell Line Information

Cell Culture Information

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Gene Information

Cat. No. CSC-RO01172
Description CHO-K1-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in CHO-K1-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, CHO-K1-Cas9 cell line can be used to efficiently generate targeted genomic modifications including gene knockout, gene knockin, gene mutagenesis, gene tagging etc. It is also an ideal cell line model for sgRNA screening and validation, either individually or in pools.
Introduction Clustered regularly interspaced palindromic repeats (CRISPR)/Cas9 is a gene-editing technology that contains two essential components: a guide RNA (gRNA) to match a target gene, and the Cas9 (CRISPR-associated protein 9) endonuclease which causes a double-stranded DNA break, allowing modifications to the genome via nonhomologous end joining (NHEJ) or homology-directed repair (HDR).
Product Type Cas9 overexpression stable cell line
Target Gene Cas9
Host Cell CHO-K1
Host Cell Species Cricetulus griseus (Chinese hamster)
Applications 1) CRISPR genome editing, such as gene knockout (KO), gene knockin (KI), gene mutagenesis, gene tagging etc.
2) High-throughput sgRNA screening and validation
Size One vial of frozen cells, typically >1x106 cells/vial
Validation T7 Endonuclease I assay
Quality Control 1) T7E1 assay
2) Mycoplasma detection
Storage Liquid nitrogen
Shipping Dry ice
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media.
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations The following safety precautions should be observed.
1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.
2. No eating, drinking or smoking while handling the stable line.
3. Wash hands after handling the stable line and before leaving the lab.
4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.
5. All waste should be considered hazardous.
6. Dispose of all liquid waste after each experiment and treat with bleach.
Ship Dry ice
Target Gene Cas9
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The CHO-K1 cell line, derived from Chinese hamster ovary cells, is a cornerstone of biomedical research and biopharmaceutical production. Renowned for its robust growth in suspension culture, high protein expression, and adaptability to serum-free culture conditions, the CHO-K1 cell line is ideal for recombinant protein therapies such as monoclonal antibodies. The Cas9 Stable Cell Line - CHO-K1 is constructed by directly integrating CRISPR-Cas9 technology into the CHO-K1 genome. This engineered cell line stably expresses the Cas9 endonuclease, eliminating the need for repeated transfection with Cas9 plasmids. Its key advantages include reduced experimental variability, stable gene editing efficiency during passage, and compatibility with complex genomic manipulations.

The Cas9 Stable Cell Line - CHO-K1 holds transformative potential in drug discovery and biomanufacturing. It enables high-throughput functional genomics screening, allowing for the rapid knockout or knock-in of genes involved in apoptosis, metabolism, or cell signaling pathways, thereby identifying novel drug targets. In biopharmaceutical development, researchers have used this cell line to genetically engineer the CHO-K1 host to enhance its productivity, such as by knocking out genes that trigger apoptosis under bioreactor stress or by inserting therapeutic cassettes at genomically safe sites. This precision reduces cloning screening time from months to weeks. Furthermore, this cell line is crucial for constructing disease models (e.g., introducing oncogenic mutations) and optimizing the glycosylation profile of biologics by editing glycosyltransferase genes. Its stability ensures the consistent performance of CRISPR in GMP-compliant large-scale manufacturing, making it an indispensable tool for developing next-generation cell therapies and biosimilars.

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Customer Reviews
Invaluable tool

The growth kinetics are excellent, and the Cas9 expression is extremely reliable, making it the perfect starting point for our protein expression optimization projects.

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