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Cas9 Stable Cell Line - ID8

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

Cat. No. :   CSC-RO01186 Host Cell :   ID8

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

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Gene Information

Cat. No. CSC-RO01186
Description ID8 -Cas9 cell line is engineered to stably overexpress Cas9 nuclease. The Cas9 nuclease in ID8 -Cas9 cell line has been functionally validated using T7 Endonuclease I assay. In combination with separately transfected sgRNAs, ID8 -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 ID8
Host Cell Species Mus musculus (Mouse)
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 Cas9 Stable Cell Line - ID8 is a genetically engineered mouse ovarian cancer cell line integrating the CRISPR-Cas9 system for targeted genome editing. Derived from the original ID8 cells (a well-established ovarian cancer research model), this stable cell line constitutively expresses the Cas9 nuclease protein. The ID8 cell line itself originates from C57BL/6 mouse ovarian surface epithelial cells, transformed with the SV40 large T antigen to acquire immunomodulatory activity, making it ideal for studying tumor microenvironment interactions. The integration of Cas9 allows researchers to bypass transient transfection steps, ensuring stable and efficient gene editing across various experiments.

This genetically engineered cell line significantly accelerates the application of functional genomics and drug development. Researchers use Cas9-ID8 cells for high-throughput CRISPR screening to identify ovarian cancer-specific oncogenes, tumor suppressor genes, and drug resistance mechanisms. Stable Cas9 expression enables the rapid construction of gene knockout/knock-in models, allowing for the validation of therapeutic targets such as PARP inhibitor responses or immunotherapy responses. Furthermore, these cells facilitate in vivo studies: when implanted into syngeneic mice, they form tumors that retain the CRISPR-editable properties, allowing for the study of the tumor microenvironment and gene function during metastasis. Beyond basic research, Cas9-ID8 simplifies preclinical testing and biomarker discovery for combination therapies, providing a versatile tool for developing personalized treatment strategies targeting the heterogeneity of ovarian cancer.

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