Product Information | |
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Product Name | Cas9 Expressing Human tongue squamous cell carcinoma cells |
Specification | 1*10^6 |
System | Eye, ear, nose, throat, and oral system |
Resistance | hygro |
Cas9 expression detection | Provided |
Cell name | HSC3-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 |
The HSC3-CAS9 is a human oral squamous cell carcinoma (OSCC)-derived cell line designed for advanced genetic engineering applications This cell line has been genetically modified to express the Cas9 nuclease a hallmark of the CRISPR/Cas9 genome editing technology Originating from the HSC3 cell line known for its relevance in cancer research HSC3-CAS9 provides a robust platform for researchers aiming to dissect the genetic underpinnings of oral cancer biology and therapeutic resistance
Cultured in a nutrient-rich environment with RPMI-1640 medium complemented with 10% fetal bovine serum (FBS) HSC3-CAS9 exhibits optimal growth characteristics conducive to extensive experimentation The stable integration of the Cas9 gene is achieved using a lentiviral vector system ensuring a high level of enzymatic expression and facilitating effective genome modifications The presence of the Cas9 expression is confirmed through specific detection methods underscoring the reliability of this cell line for precise genetic manipulations
One of the standout features of HSC3-CAS9 is its hygromycin resistance which allows for the selective maintenance of Cas9-expressing populations This characteristic empowers researchers to easily enrich for genetically modified cells while minimizing contamination from non-transduced populations Rigorous mycoplasma testing guarantees the integrity and authenticity of the cell culture ensuring that experimental results are not confounded by microbial contamination
With its ability to serve as a model for OSCC studies HSC3-CAS9 is particularly valuable for the exploration of oncogenic pathways drug resistance mechanisms and novel therapeutic strategies Its application is also pivotal for functional genomics enabling researchers to create targeted gene knockouts or insertions to elucidate critical factors in the progression and treatment of oral cancers
HSC3-CAS9 cells are conveniently shipped and stored in liquid nitrogen with precautions for dry ice transport to maintain cell viability Each vial contains approximately 1×10^6 cells ensuring an ample supply for initial experiments For optimal results a recommended passage ratio of 1:2–1:4 is specified supporting consistent growth and functionality across multiple uses
This versatile cell line is an essential tool for researchers delving into the complexities of oral squamous cell carcinoma opening avenues for innovative therapies and advancing our understanding of cancer biology As the field continues to embrace genetic engineering technologies HSC3-CAS9 stands out as a pivotal resource in the quest for effective cancer treatments
HSC3-CAS9 serves as a revolutionary tool in gene editing applications within both research and clinical settings particularly in the development and optimization of CRISPR/Cas9 techniques This product is specifically designed for targeting and modifying genomic sequences in a range of cell types including pluripotent stem cells and primary human cells thus facilitating studies in genetics oncology and regenerative medicine
Researchers can implement HSC3-CAS9 in workflows involving the knockout or activation of genes to elucidate their functions in disease models or to develop gene therapies for conditions such as sickle cell disease and muscular dystrophy By utilizing streamlined protocols such as electroporation or lipid-based transfection methods users can achieve high transfection efficiencies enabling precise editing outcomes
The practical benefits of HSC3-CAS9 include enhanced specificity and reduced off-target effects which are critical in ensuring safety and accuracy in therapeutic applications This product not only accelerates discovery but also provides a robust platform for advancing genomic studies harnessing the full potential of CRISPR technology across various experimental contexts
Please note that all services are for research use only. Not intended for any clinical use.
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