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. 2015 Jun 17;10(6):e0129072. doi: 10.1371/journal.pone.0129072

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© 2015 Jungke 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 properly credited.

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Fig 3 — (A) Scheme of the embryonic functionality assay. (B) 27 CreER^T2-driver lines are shown with respect to CreER^T2 expression at 24 hpf (CreER^T2) and the respective embryonic functionality assay indicated by native EGFP fluorescence.