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. 2015 Dec 9;15:286. doi: 10.1186/s12870-015-0674-3

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© Hou et al. 2015

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

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Fig. 4 — H3K4me2/me3 difference revealed by Western blot in the wild-type (ZH11) and jmj704-1 plants. Rabbit ployclonal antibody to Histone H3, or H3K4me2/me3 was used in Western blot. The mean signal intensity ± SD (from three biological replicates) of H3K4me2/me3 is shown as numbers normalized to the ZH11 level. The intensity of ZH11 was set to 1. Histone H3 was used as a loading control. Significance of differences between ZH11 and jmj704-1 plants was determined by Student’s t tests. *P < 0.05