Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : CSC-RO01174 Host Cell : GL261
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01174 |
| Description | GL261-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in GL261-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, GL261-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 | GL261 |
| Host Cell Species | Mus musculus (Mouse) |
| 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 |
The GL261 cell line is a mature mouse glioma model derived from chemically induced brain tumors in C57BL/6 mice. These cells exhibit characteristics of high-grade gliomas, including rapid proliferation, invasive growth patterns, and expression of typical glioma markers. The Cas9 Stable Cell Line - GL261 is a genetically engineered variant in which CRISPR-associated protein 9 (Cas9) is stably integrated into the GL261 genome. This modification allows for the sustained and inducible expression of the Cas9 endonuclease without transient transfection. This cell line maintains glioma specificity while providing a powerful platform for targeted genome editing.
The Cas9 Stable Cell Line - GL261 holds transformative potential in oncology and neuroscience research. Firstly, it can serve as a powerful tool for high-throughput CRISPR screening to identify novel therapeutic targets for glioblastoma. Researchers can efficiently perform gene knockout, knock-in, or transcriptional activation to investigate glioma-related pathways such as the EGFR signaling pathway, tumor suppression mechanisms, or angiogenesis regulators. Stable Cas9 expression facilitates longitudinal studies of tumor evolution and drug resistance mechanisms without the need for repeated transfections. Furthermore, this cell line can be used to accurately mimic human glioblastoma mutations in immunocompetent mouse models for preclinical immunotherapy testing. This cell line also holds immeasurable value in studying tumor microenvironment interactions, validating CRISPR-based therapies, and developing personalized treatment options through in vitro gene editing of patient-derived cells prior to transplantation.
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The cells maintain excellent morphology and growth kinetics while providing high knockout efficiency. It’s an ideal tool for our syngeneic mouse model experiments.
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