Selected article for: "fluorescence signal and high signal"

Author: A. Reiser; D. Woschée; N. Mehrotra; R. Krzyszton; H. H. Strey; J. O. Rädler
Title: Correlation of mRNA delivery timing and protein expression in lipid-based transfection
  • Document date: 2019_4_13
  • ID: 9h6ctbyx_30
    Snippet: Single-cell microarrays were produced by microscale plasma-induced protein patterning (µPIPP) like already described elsewhere (38, 39) . The array consists of a micropattern with cell adhesive squares, which are coated with fibronectin. The interspace between the squares is passivated with PLL-g-PEG. By cell adhesion to the squares the cells align on the micropattern enabling high-throughput read out of each cellular fluorescence signal. The wh.....
    Document: Single-cell microarrays were produced by microscale plasma-induced protein patterning (µPIPP) like already described elsewhere (38, 39) . The array consists of a micropattern with cell adhesive squares, which are coated with fibronectin. The interspace between the squares is passivated with PLL-g-PEG. By cell adhesion to the squares the cells align on the micropattern enabling high-throughput read out of each cellular fluorescence signal. The whole array has six channels with the described micropattern on the bottom of each channel.

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