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-RO01184 Host Cell : HTR-8/SVneo
Size : >1x106 cells/vial Validation : T7 Endonuclease I assay
| Cat. No. | CSC-RO01184 |
| Description | HTR-8/SVneo-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in HTR-8/SVneo-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, HTR-8/SVneo-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 | HTR-8/SVneo |
| 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 - HTR-8/SVneo is an immortalized human trophoblast cell line derived from placental tissue in early pregnancy. This cell line was initially established through transfection with simian virus 40 large T antigen (SV40 TAg), preserving key characteristics of extravillous trophoblast cells, including invasiveness and hormone secretion. The Cas9-stable cell line—HTR-8/SVneo—is a genetically engineered variant in which the CRISPR-associated protein 9 (Cas9) endonuclease is stably integrated into the genome. Parental HTR-8/SVneo cells exhibit epithelial-like morphology, express trophoblast-specific markers (such as cytokeratin-7 and HLA-G), and demonstrate robust proliferative capacity, making them ideal for placental research. Cas9 modification enables precise genome editing while preserving the biological relevance of the original cell line in mimicking early pregnancy development.
The Cas9 Stable Cell Line - HTR-8/SVneo provides a powerful platform for functional genomics and disease modeling in reproductive biology. Researchers have used it for high-throughput CRISPR screening to identify genes regulating trophoblast cell invasion, proliferation, and differentiation—processes crucial for placental establishment and disrupted in pathological conditions such as preeclampsia and fetal growth restriction. Stable Cas9 expression simplifies knockout/knock-in studies of pregnancy-related genes (such as FLT1, ENG, or HIF pathway components) by avoiding transfection variability. Furthermore, this cell line can aid in studying the mechanisms of maternal-fetal interface interactions, including trophoblast cell responses to oxidative stress, hypoxia, or immunomodulators. Its pharmaceutical applications include screening for therapeutics against placental dysfunction and assessing the toxicity of compounds during pregnancy.
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We are very impressed with the HTR-8/SVneo Cas9 stable cell line. It has proven to be a reliable and robust model for our studies on trophoblast function and placental development using CRISPR/Cas9 technology.
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