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Figure 4
Micrographs of the trapping region obtained using trans-illumination. In (a), chemically fixed macrophages are inserted into the microfluidic channel. Single cells are clearly visible in this imaging mode, as can be seen from the inset. (b) Upon laser trapping, the cell is pulled into the trap center. Light scattering from the walls of the capillary and from the trapped cell is clearly visible. Here, a trapping power of 100 mW was used.

Journal logoJOURNAL OF
SYNCHROTRON
RADIATION
ISSN: 1600-5775
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