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. 2016 Jul 7;66(4):522–529. doi: 10.1270/jsbbs.16011

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Copyright © 2016 by JAPANESE SOCIETY OF BREEDING

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 work is properly cited.

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Fig. 4 — PCR amplification patterns generated by SSR markers. M 500 bp marker, 1 Ae. variabilis, 2 Yiyuan 2, 3 N2BT2D, 4 N2DT2B, 5 NZ272, 6 NZ266, 7 NZ286, 8 NZ292, 9 NZ294, 10 NZ298, 11NZ304, 12 NZ306, 13 NZ307, 14 NZ311, 15 NZ309, 16 NZ281, 17 NZ283, 18 NZ321, 19 NZ323. 5, 16 and 17 were 2S^v addition lines; 6, 7, 8, 9 and 10, 2S^v(2B) substitution lines; 11, 12, 13, 14, 18 and 19, 2S^v(2D) substitution lines; 15 common wheat without an alien chromosome. Markers gwm148, cfd51 and gdm107 were the specific markers for 2D; markers wmc592 and barc18 were specific for 2B.