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-RO01163 Host Cell : ARPE-19
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01163 |
| Description | ARPE-19-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in ARPE-19-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, ARPE-19-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 | ARPE-19 |
| 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—ARPE-19—is a genetically engineered human retinal pigment epithelium cell line derived from the parental ARPE-19 cells, which were originally isolated from the retina of an adult human donor. This cell line has been modified to stably express the CRISPR-associated protein 9 (Cas9) endonuclease—a key component of the CRISPR-Cas9 genome editing system. The stable integration of the Cas9 gene ensures continuous and long-term expression of the enzyme, thereby eliminating the need for repetitive transfection procedures. ARPE-19 cells are highly valued for their distinct epithelial morphology, their capacity for polarization, and their functional characteristics, which closely mimic those of native retinal pigment epithelium (RPE) cells.
Researchers can utilize this cell line to perform targeted gene knockouts, knock-ins, or transcriptional activation within retinal disease models, thereby gaining deeper insights into the pathogenesis of conditions such as Age-Related Macular Degeneration (AMD), Retinitis Pigmentosa, and Diabetic Retinopathy. The stable expression of Cas9 significantly streamlines high-throughput CRISPR screening workflows, enabling researchers to systematically identify key genes involved in RPE function, oxidative stress responses, and angiogenesis. Furthermore, this cell line accelerates the drug discovery and development process by facilitating the rapid validation of therapeutic targets within a physiologically relevant cellular system. Its excellent compatibility with cutting-edge technologies—such as live-cell imaging, electrophysiology, and co-culture systems—further facilitates in-depth investigations into intercellular interactions, barrier function, and drug delivery mechanisms.
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The cells behave exactly like the parental line but with the added benefit of consistent Cas9 expression, which is vital for our vision research.
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