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-RO01205 Host Cell : MGC803
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01205 |
| Description | MGC803-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in MGC803-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, MGC803-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 | MGC803 |
| Host Cell Species | Homo sapiens (Human) |
| 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 MGC803 cell line is a human gastric cancer cell line established from tumor tissue of gastric cancer patients. It is an important model for studying the biology, molecular mechanisms, and therapeutic interventions of gastric cancer. The Cas9 Stable Cell Line - MGC803 is obtained through genetic engineering of this parent cell line, enabling it to stably express CRISPR-associated protein 9 (Cas9). This cell line maintains the stability of Cas9 protein expression during passage, allowing for efficient and reproducible genome editing without repeated transfections. Key features of this cell line include high editing efficiency, compatibility with single-guide RNA (sgRNA) delivery for targeted modification, and preservation of the original phenotype of MGC803 cells—making it ideal for loss-of-function studies, gene knockout validation, and functional genomics screening in gastric cancer research.
The Cas9 Stable Cell Line - MGC803 is widely used in multiple fields of oncology and genetics research. It enables high-throughput CRISPR screening to identify key genes, drug targets, or drug resistance mechanisms in gastric cancer, and allows for genome-wide or pathway analysis using mixed sgRNA libraries. In drug development, this cell line helps construct homologous knockout models (e.g., TP53, KRAS, or CDH1 mutations), enabling the evaluation of treatment efficacy and resistance patterns within a controlled genetic context. It also supports functional validation of tumor suppressor genes, oncogenes, and signaling pathways through precise gene knockout, knock-in, or base editing, thereby accelerating research into the mechanisms of gastric cancer progression and metastasis. Furthermore, this cell line plays a crucial role in synthetic lethality screening, biomarker identification, and the construction of personalized cancer models through patient-derived xenograft (PDX) engineering.
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We are very impressed with the high knockout efficiency achieved using the MGC803 Cas9 stable line. It allowed us to move straight to gRNA transfection without worrying about Cas9 expression levels.
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