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. 2018 Aug 14;19(8):2403. doi: 10.3390/ijms19082403

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© 2018 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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DlMFT expression in response to abiotic stress. EC was treated with nutrient solution containing 150 mM NaCl or PEG-4000 for different times, KClO₃ at the indicated concentrations, or exposed to different light qualities. RNA was isolated from samples treated with: (A) 150 mM NaCl (0, 1, 2, 4, 8, 12 and 16 h), (B) PEG-4000 (0, 1, 2, 4, 8, 12, 16 and 24 h), (C) different light qualities (dark, red, green, blue, and white) for 24 h, (D) KClO₃ (0.25, 0.5, 1 and 3 mM/L), (E) different temperature (25, 32, 34, 36 and 40 °C), (F) sucrose (0, 0.1, 0.5, 1.0, 2.0, 4.0 and 6.0%). Reference genes were EF1a, FSD, and elf4a. Data are means ± SD (n = 3).

DlMFT expression in response to abiotic stress. EC was treated with nutrient solution containing 150 mM NaCl or PEG-4000 for different times, KClO₃ at the indicated concentrations, or exposed to different light qualities. RNA was isolated from samples treated with: (A) 150 mM NaCl (0, 1, 2, 4, 8, 12 and 16 h), (B) PEG-4000 (0, 1, 2, 4, 8, 12, 16 and 24 h), (C) different light qualities (dark, red, green, blue, and white) for 24 h, (D) KClO₃ (0.25, 0.5, 1 and 3 mM/L), (E) different temperature (25, 32, 34, 36 and 40 °C), (F) sucrose (0, 0.1, 0.5, 1.0, 2.0, 4.0 and 6.0%). Reference genes were EF1a, FSD, and elf4a. Data are means ± SD (n = 3).