Skip to main content
. Author manuscript; available in PMC: 2019 Sep 13.
Published in final edited form as: Lab Chip. 2019 Mar 13;19(6):941–947. doi: 10.1039/c8lc01310a

Fig. 6.

Fig. 6

Green fluorescence (SYTO 9) and red fluorescence (PI) plot of the bacterial cells from liquefied stool samples prepared by (A) a standard stool-liquefaction process and (B) our acoustofluidic stool liquefier. SYTO 9, a membrane permeable stain, is employed to identify live bacterial cells while PI, a membrane impermeable stain, is used to identify dead bacterial cells. The percentage of live bacterial cells was 39.1% and 45.1% for (A) and (B), respectively.