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. 2021 Mar 8;12:625670. doi: 10.3389/fpls.2021.625670

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Copyright © 2021 Braglia, Lauria, Appenroth, Bog, Breviario, Grasso, Gavazzi and Morello.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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PCR amplification of all clones of the Lemna minor group with primers TUBB 23-11-1. From left to right: Lemna turionifera: 9434, BOG0006, 9530; L. minor-SC I: LM0010, LM0011, 8744, 5500, 7766, 9536, 8623, 7753, 7194, 8292, 7022, 9495, 9252, 9441, KJA0013, LM0008, 7210, 9533; L. minor-SC II: 8627, 8676, 8695, 9017, 9257, 9283, LM0005, LM0004, 9436b, 9580, LM0006, 9481, LM0007, 9437, KJA0017, KJA0016, 9355, 9440, 8389, 8625; Lemna gibba: 7796 and 7742a. The A and B arrows indicate the L. turionifera and L. minor bands, respectively. A molecular weight size marker (M) is reported on the left.