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To duplicate 60 mm dishes, either 1 μM Epoxomicin (#24801, EMD), 10 μM MG132 or vehicle (DMSO) was added directly to the cell medium, starting 3 hr after UVB treatment and subsequently after an additional 2 and 5 hr. Cells were collected at the indicated times and then lysed in loading buffer for Western blot analysis.
Copyright and License information: ©2018 Wu et al
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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