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. Author manuscript; available in PMC: 2012 May 1.
Published in final edited form as: J Pharmacol Toxicol Methods. 2010 Nov 25;63(3):217–222. doi: 10.1016/j.vascn.2010.11.003

Table 1.

Average fold-increase values for HEK293 cells expressing P-gp, MRP1 or ABCG2 as measured by flow cytometer or cell counter.

Transporter Fold-increase
Cell counter Flow cytometer p
P-gp 10.0±5.0 27.5±9.0 0.0085
MRP1 3.7±1.5 4.1±0.9 0.61
ABCG2 2.3±0.9 3.1±0.8 0.22

Fold-increase was determined by dividing intracellular fluorescence determined in cells incubated with substrate in the presence of inhibitor alone by intracellular fluorescence determined in the presence of substrate alone. Substrate/inhibitor pairs were rhodamine/valspodar, calcein AM/MK571, and BODIPY-prazosin/FTC for P-gp, MRP1, and ABCG2, respectively. Mean ± standard deviation is shown; p values were determined by Students t-test between average fold-increase values measured by flow cytometer or cell counter. p < 0.05 was considered significant.