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. 2013 Sep 12;3:2640. doi: 10.1038/srep02640

Figure 3. Analysis of mitotic entry by live cell imaging.

Figure 3

Cells growing in glass bottom dishes were synchronised by double thymidine block and released in panobinostat or excipient control medium. 3 hours following release, cells were placed in a heated chamber and imaged using a 20× objective every 2 minutes. The representative images shown were taken at the stated time points following release.