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-RO01168 Host Cell : BJ
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01168 |
| Description | BJ-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in BJ-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, BJ-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 | BJ |
| 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 Cas9 stable cell line-BJ is a genetically engineered human fibroblast cell line derived from the primary BJ cell line, which originates from normal neonatal foreskin tissue. This cell line has been modified to stably express the Streptococcus pyogenes Cas9 nuclease, a key component of the CRISPR-Cas9 genome editing system. Through lentiviral transduction and antibiotic selection, these cells maintain stable Cas9 expression during passage, ensuring reliable gene editing without the need for repeated transfections. The BJ parental cell line exhibits typical fibroblast morphology, adherent growth characteristics, and a diploid karyotype, making it ideal for studying human cellular processes in non-cancer environments.
The Cas9 stable cell line-BJ holds broad application potential in biomedical research, particularly in functional genomics and therapeutic drug development. Researchers utilize this cell line for highly efficient gene knockout studies, where guide RNA (gRNA) targets specific genes to investigate loss-of-function phenotypes in areas such as DNA repair, aging, or metabolic pathways. This cell line is compatible with array-based or hybrid CRISPR screening and can be used to identify genes involved in disease mechanisms, such as cancer progression or neurodegenerative diseases, across the entire genome. Furthermore, this cell line facilitates precise gene knock-in experiments, inserting reporter tags, disease-related mutations, or therapeutic transgenes via homologous recombination repair (HDR). In drug discovery, this cell line can serve as a tool for validating drug targets by constructing homologous cell models with engineered mutations and evaluating the efficacy of compounds.
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The Cas9-BJ fibroblast line from Creative Biogene has proven to be an excellent tool for our aging research. It’s often difficult to maintain stability in primary-like cells, but this line has remained consistent and highly efficient for all our CRISPR-based gene editing needs.
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