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Cas9 Stable Cell Line - ISHIKAWA

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RO01189 Host Cell :   Ishikawa

Size :   >1x106 cells/vial Validation :   T7 Endonuclease I assay

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Cell Line Information

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Gene Information

Cat. No. CSC-RO01189
Description ISHIKAWA-Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in ISHIKAWA-Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, ISHIKAWA-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 Ishikawa
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
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The ISHIKAWA cell line is a mature human endometrial adenocarcinoma cell line derived from endometrial cancer patients. Due to its epithelial origin, hormone sensitivity, and relevance to gynecological cancers, this cell line is widely used in oncology and molecular biology research. The Cas9 Stable Cell Line - ISHIKAWA is a genetically engineered variant in which CRISPR-associated protein 9 (Cas9) is stably integrated into the genome. This modification allows for stable and efficient gene editing without transient transfection, ensuring continuous expression of Cas9 during cell passage.

The Cas9 Stable Cell Line - ISHIKAWA is a powerful tool for functional genomics and cancer research. Researchers use it to study gene function in the pathogenesis of endometrial cancer through targeted knockout or mutation, such as tumor suppressor genes (e.g., PTEN) or oncogenes (e.g., PIK3CA). It facilitates high-throughput CRISPR screening to identify novel therapeutic targets or drug resistance mechanisms in hormone-driven cancers. Furthermore, this cell line is well-suited for studying estrogen and progesterone signaling pathways, providing insights into hormone receptor interactions and drug responses. Beyond oncology, it supports research on DNA repair mechanisms, apoptosis regulation, and metastasis. Its stable Cas9 expression simplifies workflows, reduces experimental variability and costs associated with repeated transfections, thereby accelerating drug discovery and personalized medicine.

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Customer Reviews
A Reliable Tool for Endometrial Cancer Research

The Cas9 activity is robust and stable, making our gene knockout experiments much more reproducible compared to transient transfection methods. Highly recommended for hormonal signaling studies.

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