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. 2017 Feb 28;112(4):795–804. doi: 10.1016/j.bpj.2016.12.045

Figure 1.

Figure 1

Schematics of experimental setup. (A) Top and cross views of the microfluidics device for delivering ATP solution to cultured fibroblast (NIH 3T3) cells. Inset: Fluorescent calcium imaging of a typical experiment. (B) Relative fluorescent intensities indicating the calcium dynamics, Ri(t), of individual cells (dashed lines) when stimulated by external ATP at four different concentrations, and the average trajectories (solid lines) at each concentration. To see this figure in color, go online.