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:
    1. Name: CL1-0
    2. Name: H1299
      Description: Human non-small cell lung adenocarcinoma
    3. Name: HEK-293
      Description: Human embryonic kidney Fibroblast
      Known as: HEK293, 293
    4. Name: HeLa
      Description: Human cervix epitheloid carcinoma cells
    5. Name: Hep G2
      Description: Human hepatocarcinoma cells
    6. Name: Hep-2
      Description: Human cervix epitheloid carcinoma cells, HeLa-derivative
    7. Name: MDCK
      Description: Canine kidney epithelial cells
    8. 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.

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