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-RO01200 Host Cell : MC38
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01200 |
| Description | MC38-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in MC38-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, MC38-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 | MC38 |
| 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 MC38 cell line is a mouse colon adenocarcinoma model derived from C57BL/6 mice. Due to its potent tumorigenicity and immunogenicity, it is widely recognized in preclinical cancer research. As a homologous cell line, MC38 can stably form tumors in immunocompetent normal mice, thus possessing significant value in studying tumor-immune interactions, immunotherapy efficacy, and metastasis. The Cas9 Stable Cell Line - MC38 is a genetically engineered variant in which CRISPR-associated protein 9 (Cas9) is stably integrated into the MC38 genome. This modification allows for precise targeted genome editing without repeated transfections because the cells constitutively express the Cas9 nuclease. This cell line ensures stable Cas9 expression and retains key characteristics of the parental MC38, including rapid proliferation, epithelial cell morphology, and sensitivity to immune checkpoint inhibitors.
The Cas9 Stable Cell Line - MC38 is widely used in various applications in oncology and immunology research. It serves as a powerful platform for functional genomics, supporting high-throughput screening to identify genes crucial for tumor growth, metastasis, or immune escape. Researchers have used this cell line to construct homologous knockout models of specific oncogenes (such as Kras and Myc) or tumor suppressor genes (such as P53) to conduct research on carcinogenesis mechanisms and drug resistance. In immunotherapy development, this cell line facilitates research on these pathways by constructing precise gene perturbations to assess the impact of immune checkpoint pathways (such as PD-1/PD-L1 or CTLA-4) on T cell activation and tumor clearance.
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Creative Biogene’s MC38 Cas9 line is by far the best we’ve used. It grows quickly and maintains a very high level of Cas9 expression, which is perfect for our large-scale CRISPR screens in syngeneic tumor models.
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