Figure 1.
a) A schematic illustration of the method of forming droplets for protein crystallization trials in a PDMS/glass capillary composite microfluidic device. b) A photograph of the composite device. All inlets and channels were filled with [Fe(SCN)x](3−x)+ solution for clarity. c) A microphotograph of thaumatin crystals grown inside droplets in a capillary. Droplets were generated by the method illustrated in (a).