Clonogenic assay

WH Wan Gi Hong
JK Ju Yeon Kim
JC Jeong Hyun Cho
SH Sang-Gu Hwang
JS Jie-Young Song
EL EunAh Lee
TC Tong-Shin Chang
HU Hong-Duck Um
JP Jong Kuk Park
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Clonogenic assays were performed as described previously [42]. NCI-H460 and NCI-H1299 cells were seeded in 60 mm dishes in triplicate at densities estimated to yield 20-100 colonies/dish (100, 200, 400, 600 and 1000 cells/dish). After 24 h incubation, cells were pre-incubated with or without 10 or 30 μM AMRI-59 for 16 h and exposed to different doses of IR (1, 3, 5, 7 Grey [Gy]) using 137Cs as the radiation source (Atomic Energy of Canada, Ltd., Ontario, Canada). Treated and control cells were cultured for 10-14 days, and colonies >200 μm in diameter counted using a colony counter (Imaging Products, VA, USA). Dose enhancement ratio (DER) values were calculated with Excel program (Microsoft Co. USA) as describe in Table Table11.

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