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. 2017 Dec 28;69(5):1109–1123. doi: 10.1093/jxb/erx444

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© The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 3. — Expression analysis and subcellular localization of AaAPK1. (A) The expression levels of AaAPK1 in under treatment with ABA, drought (air-drying), and NaCl. (B) The tissue profiles of AaAPK1. (C) Subcellular localization of AaAPK1. The coding sequence of AaAPK1 was in-frame fused with YFP, and under the control of the 35S promoter, then transferred into A. tumefaciens GV3101 and infiltrated into leaves of N. benthamiana. DAPI-stained nuclei were used as the control. (This figure is available in colour at JXB online.)