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. 2018 May 8;18:82. doi: 10.1186/s12870-018-1290-9

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© The Author(s). 2018

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. 8 — Results of PCR analysis using the F2 and R2 primer pair (BoMYBL2v-F and BoMYBL2v-R) to amplify BoMYBL2–1v, which contains the substituted region of the promoter. The white arrow indicates the position of the predicted PCR product. Three purple cabbages (Purple B, NP-J-156, and HK-047) were heterozygous (BoMYBL2–1v/BoMYBL2–1sub), but B90 was homozygous for BoMYBL2–1v. All other purple cabbages were homozygous for BoMYBL2–1sub