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Cells were plated in 96‐well plates at a concentration of 5 × 104 cells/mL for 24 hours. Caspase‐Glo 3/7 Reagent (Promega) was added to each well. After being gently mixed with a plate shaker, cells were incubated at room temperature. Finally, luminescence of each sample was measured in a plate‐reading luminometer.
Copyright and License information: ©2021 The Authors. published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
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