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-RO01191 Host Cell : Jurkat, Clone E6-1
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01191 |
| Description | Jurkat, Clone E6-1-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in Jurkat, Clone E6-1-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, Jurkat, Clone E6-1-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 | Jurkat, Clone E6-1 |
| 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 Jurkat, Clone E6-1 cell line is a mature human T lymphocyte line originally derived from the peripheral blood of a 14-year-old male with T-cell leukemia. This immortalized cell line exhibits characteristics of immature T cells, expressing CD3 and CD4 markers but not CD8. It grows vigorously in suspension culture, responds to T cell activators such as phytohemagglutinin (PHA), and demonstrates good reproducibility, making it a cornerstone of immunology, oncology, and HIV research. The Cas9 Stable Cell Line - Jurkat, Clone E6-1 is further developed through transduction of stably expressed Cas9 nuclease. This genetically engineered variant achieves precise, programmable genome editing while maintaining the growth kinetics and phenotypic characteristics of the parent cell line. Stable Cas9 expression eliminates the need for repeated transfections, ensuring consistent editing efficiency during passage and reducing experimental errors.
In functional genomics, Cas9 Stable Cell Line - Jurkat, Clone E6-1 enables high-throughput CRISPR screening to identify genes regulating T-cell activation, cytokine production, and immune checkpoint pathways, thereby accelerating drug target discovery for autoimmune diseases and cancer. Oncology researchers use it to mimic T-cell leukemia mutations (e.g., NOTCH1 or PTEN knockout) and investigate chemotherapy resistance mechanisms. In immunotherapy development, it helps knock out genes such as PD-1 or CTLA-4 to enhance the efficacy of CAR-T cells or study immune escape mechanisms. Infectious disease research uses it to elucidate host factors in viral infections (e.g., studying HIV invasion by knocking out CCR5) or to construct reporter gene cell lines for pathogen lifecycle monitoring. Compared to transient CRISPR systems, this stable cell line offers superior reproducibility, making it suitable for long-term studies such as tumor xenograft models or chronic toxicity trials, thus becoming an essential tool for preclinical validation of gene therapy and immunomodulatory drugs.
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Editing suspension cells can be challenging, but this Jurkat Clone E6-1 Cas9 line made the process seamless. The stability of Cas9 expression is outstanding, allowing us to perform complex CRISPR screens with high confidence and minimal background noise.
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