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. 2016 Feb 17;11(2):e0149184. doi: 10.1371/journal.pone.0149184

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© 2016 Even 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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Fig 6 — GFP-cyclin K and HA-cyclins L1 and L2 were expressed in HeLa cells and their localizations were analysed by fluorescence microscopy using respectively GFP-cyclin K (A) or immunofluorescence with anti-cyclin L1 (D) and L2 (G) antibodies. Localizations were compared with the one of endogenous PTB (B,E,H). Respective merge images (C,F,I) show an absence or a very poor co-localization of cyclins with CDK13 in PNC. An increased magnification of merge labelling is inserted in C and I. Scale bar: 5μm.