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• W3036954442 endingPage "1482" @default.
• W3036954442 startingPage "1482" @default.
• W3036954442 abstract "Single-cell cloning (SCC) is a critical step in generating monoclonal cell lines, which are widely used as in vitro models and for producing proteins with high reproducibility for research and the production of therapeutic drugs. In monoclonal cell line generation, the development time can be shortened by validating the monoclonality of the cloned cells. However, the validation process currently requires specialized equipment that is not readily available in general biology laboratories. Here, we report a disposable SCC device, in which single cells can be isolated, validated, and expanded to form monoclonal cell colonies using conventional micropipettes and microscopes. The monoclonal cells can be selectively transferred from the SCC chip to conventional culture plates, using a tissue puncher. Using the device, we demonstrated that monoclonal colonies of actin-GFP (green fluorescent protein) plasmid-transfected A549 cells could be formed in the device within nine days and subsequently transferred to wells in plates for further expansion. This approach offers a cost-effective alternative to the use of specialized equipment for monoclonal cell generation." @default.
• W3036954442 created "2020-06-25" @default.
• W3036954442 creator A5000202149 @default.
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• W3036954442 date "2020-06-18" @default.
• W3036954442 modified "2023-10-18" @default.
• W3036954442 title "A Microfluidic Single-Cell Cloning (SCC) Device for the Generation of Monoclonal Cells" @default.
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• W3036954442 doi "https://doi.org/10.3390/cells9061482" @default.
• W3036954442 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7349811" @default.
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• W3036954442 hasPublicationYear "2020" @default.
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