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-RO01169 Host Cell : BV2
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01169 |
| Description | BV2-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in BV2-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, BV2-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 | BV2 |
| 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 Cas9 Stable Cell Line - BV2 is a genetically engineered BV2 mouse microglia cell line that stably expresses CRISPR-associated protein 9 (Cas9). The BV2 cell line originates from primary microglia of C57/BL6 mice, is immortalized through retroviral transformation, and exhibits key microglia characteristics, including phagocytic activity, cytokine secretion, and morphological plasticity. Cas9 integration is achieved via lentiviral transduction or plasmid transfection, followed by antibiotic selection to ensure stable genome integration. This cell line constitutively expresses Cas9 under the control of a strong promoter, thus maintaining nuclease activity without repeated transfection. The cell line has been rigorously validated to maintain microglia markers such as Iba1 and CD11b and exhibits strong proliferative capacity.
This Cas9 Stable Cell Line - BV2 revolutionizes research in neuroimmunology and neurodegenerative diseases. It enables high-throughput CRISPR screening to identify genes regulating microglia activation (M1/M2 polarization), phagocytosis, and inflammatory responses to stimuli such as LPS or β-amyloid. Researchers have used this cell line to construct Parkinson''s and Alzheimer''s disease models by knocking out target genes such as TREM2 or NLRP3, elucidating the roles of these target genes in neuroinflammation and neuronal death. In drug development, this cell line can facilitate rapid target validation (e.g., testing small-molecule inhibitors targeting microglia-specific pathways) and toxicity assessment. Furthermore, the Cas9-BV2 cell line simplifies modeling of similar in vivo diseases in preclinical studies, reduces dependence on primary cells, and ensures genetic consistency.
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We’ve had great success using the Cas9-BV2 cell line for studying microglial activation. The cells are easy to culture and the Cas9 expression is powerful enough to achieve near-total knockouts in our target genes. It has greatly accelerated our neurobiology projects.
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