Product Information | |
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Product Name | Cas9 Expressing Human nasopharyngeal carcinoma cells |
Specification | 1*10^6 |
System | Eye, ear, nose, throat, and oral system |
Resistance | hygro |
Cas9 expression detection | Provided |
Cell name | CNE1-CAS9 |
Cell morphology | Epithelial like, adherent cells |
passage ratio | 1:3~1:5 |
Species expression gene | Human |
Expressed Gene | Cas9 |
Properties | |
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Construction method | Viral method |
Mycoplasma detection | negative |
Storage and transportation | Dry ice transportation; Store in liquid nitrogen |
Culture system | 90% DMEM+10% FBS |
CNE1-CAS9 is an innovative and specialized cell line derived from human colorectal cancer (CRC) tissues meticulously engineered to constitutively express the Cas9 nuclease This product facilitates groundbreaking CRISPR/Cas9-based genome-editing applications specifically tailored for the study of colorectal cancer biology and therapeutic strategies The source cells are maintained in a standardized culture medium enriched with 10% fetal bovine serum (FBS) ensuring optimal growth under standard laboratory conditions
The stable integration of the Cas9 gene in CNE1-CAS9 is achieved through a lentiviral delivery system which promotes consistent expression and functional reliability The cell line exhibits robust performance in gene editing experiments providing researchers with a valuable tool for exploring genomic alterations associated with colorectal cancer Importantly the presence of hygromycin resistance allows for effective selection and expansion of Cas9-expressing cells facilitating experimental rigor and reproducibility
CNE1-CAS9 cells are crucial for a spectrum of applications including but not limited to gene function elucidation pathway characterization and validation of potential therapeutic targets pertinent to CRC The ability to employ CRISPR/Cas9 technology within this context contributes significantly to advancing personalized medicine approaches for colorectal cancer as researchers can dissect the functional roles of specific genes implicated in tumorigenesis and metastasis
To ensure experimental integrity CNE1-CAS9 cells undergo routine mycoplasma testing verifying their quality and suitability for sensitive genetic studies The cells are conveniently packaged and shipped in liquid nitrogen with transportation provided on dry ice to maintain viability and are delivered at a density of 1×10^6 cells per vial With optimal passage ratios of 1:3 to 1:5 recommended CNE1-CAS9 is designed for scalability enabling long-term studies and extensive screening processes in cancer research
In summary CNE1-CAS9 stands out as a significant tool for the scientific community empowering researchers to investigate the complexities of colorectal cancer through advanced genome-editing technologies Its unique composition and targeted applications not only enhance understanding of cancer biology but also hold promise for the development of novel therapeutic interventions
CNE1-CAS9 is primarily utilized in gene editing applications across research clinical and industrial settings where precision and efficiency are paramount It excels in enabling targeted genome modifications in a variety of organisms including mammalian cells plants and microorganisms Specific use cases include developing CRISPR/Cas9-mediated knockouts or knock-ins to study gene function disease modeling and creating genetically modified organisms for biotechnological applications
Researchers and clinicians can seamlessly integrate CNE1-CAS9 into their workflows by employing standardized protocols for simultaneous target site identification and delivery through plasmid systems or RNP complexes Its high specificity minimizes off-target effects resulting in cleaner gene edits while its robust delivery mechanisms enhance transfection efficiency crucial for sensitive cell types
The practical benefits of CNE1-CAS9 include streamlined experimental design reduced turnaround time for gene modification projects and improved reproducibility of results Additionally it is particularly well-suited for multiplex genome editing applications allowing for the concurrent modification of multiple genes thereby accelerating research in functional genomics and therapeutic development
Please note that all services are for research use only. Not intended for any clinical use.
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