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. 2020 Sep 18;11:70. doi: 10.1186/s13229-020-00376-9

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Successful maternal Ube3a gene activation upon Nestin-Cre-mediated deletion of the transcriptional STOP cassette. a, b Western blot data and UBE3A quantification from total lysates of E9 and E15 brains of Ube3a^mLSL+, Ube3a^mLSL/− mice, and WT littermates normalized to WT E15 levels. Bars depict mean ± SD (n = 2 per genotype, per time point). c, d DAB and immunofluorescent pictures of UBE3A expression in sections of brains from adult wild-type, Ube3a^mLSL/Cre⁺ and Ube3a^mLSL/Cre⁻ mice