Citation
- Authors: Chang, F. H., Lee, C. H., Chen, M. T., Kuo, C. C., Chiang, Y. L., Hang, C. Y., Roffler, S.
- Year: 2004
- Journal: Nucleic Acids Res 32 e33
- Applications: in vitro / DNA / jetPEI
- Cell types:
- Name: CL1-0
- Name: H1299
Description: Human non-small cell lung adenocarcinoma - Name: HEK-293
Description: Human embryonic kidney Fibroblast
Known as: HEK293, 293 - Name: HeLa
Description: Human cervix epitheloid carcinoma cells - Name: Hep G2
Description: Human hepatocarcinoma cells - Name: Hep-2
Description: Human cervix epitheloid carcinoma cells, HeLa-derivative - Name: MDCK
Description: Canine kidney epithelial cells - Name: NIH/3T3
Description: Murine embryonic fibroblasts
Known as: NIH/3T3, 3T3
Abstract
Efficient high-throughput expression of genes in mammalian cells can facilitate large-scale functional genomic studies. Towards this aim, we developed a simple yet powerful method to deliver genes into cells by cationic polymers on the surface of substrates. Transfection can be achieved by directly contacting nucleic acid-cell mixtures with the cationic substrates, e.g. polyethylenimine/collagen-coated wells. This single-step matrix-surface- mediated transfection method, termed 'surfection', can efficiently deliver multiple plasmids into cells and can successfully assay siRNA-mediated gene silencing. This technology represents the easiest method to transfer combinations of genes in large-scale arrays, and is a versatile tool for live-cell imaging and cell-based drug screening.