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. 2016 Dec 5;6:38376. doi: 10.1038/srep38376

Figure 3. Cell viability assay within the device.

Figure 3

Human embryonic kidney HEK-293 cells were seeded and grown in the cell culture channel of the Matrigel-loaded device under the 2–10% FBS gradient with a flow rate of 3 μL/h. After 3 days (upper) and 5 days (lower) of culture, the cells were subjected to live/dead staining. Living cells were stained green by calcein-AM, and dead cells were stained red by PI (original magnification ×100).