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-RO01187 Host Cell : IPEC-J2
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01187 |
| Description | IPEC-J2-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in IPEC-J2-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, IPEC-J2-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 | IPEC-J2 |
| Host Cell Species | Sus scrofa (Pig) |
| 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 IPEC-J2 cell line is a non-transformed intestinal epithelial cell line derived from the jejunum of newborn piglets. It is an important in vitro model for studying porcine intestinal physiology, barrier function, and host-pathogen interactions, and is applied in porcine biology and comparative biology. The Cas9 Stable Cell Line - IPEC-J2 is a genetically engineered variant in which CRISPR-associated protein 9 (Cas9) has been stably integrated into the genome of IPEC-J2 cells. This modification allows for stable and efficient genome editing without transient transfection of the Cas9 component. Stable expression of Cas9 reduces experimental variability, simplifies gene knockout or knock-in studies, and makes it ideal for high-throughput screening. These cells retain key characteristics of the parent cell line, including epithelial morphology, polarization, and barrier integrity, while providing a powerful platform for precise gene manipulation.
The Cas9 Stable Cell Line - IPEC-J2 is widely used to study intestinal diseases such as inflammatory bowel disease (IBD), necrotizing enterocolitis (NEC), and viral/bacterial infections (e.g., rotavirus or Salmonella infections). Researchers have used this cell line to construct specific gene knockout models involving immune responses (such as TLRs or cytokines), nutrient transporters, or tight junction proteins, thereby elucidating their roles in intestinal barrier dysfunction. Furthermore, this cell line can aid in drug development by screening compounds that modulate epithelial repair or pathogen resistance. In toxicology, it helps assess the effects of environmental toxins, feed additives, or nanomaterials on gut health. The cell line also supports research on host-microbiome interactions, allowing for targeted editing to explore how gut microbes influence epithelial gene expression.
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The cells are healthy, and the stable Cas9 expression is perfect for studying intestinal pathogens and host-gene interactions.
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