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. 2015 Mar 7;66(9):2733–2748. doi: 10.1093/jxb/erv069

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© The Author 2015. 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/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 3. — BiFC confirms the interaction of OsCNIH1 with OsHKT1;3 and demonstrates the likely oligomerization of OsCNIH1 in transiently transfected tobacco leaves. (A, E) Reciprocal interaction between YFC–OsCNIH1/YFN–OsHKT1;3 and YFN–OsCNIH1/YFC–OsHKT1;3 confirms the interaction of the two proteins in the ER. (B) Co-expression of YFC–OsCNIH1 and YFN–-OsCNIH1 indicates the possible oligomerization of cornichon in the ER. Absence of a fluorescence complementation signal indicates that: OsCNIH1 does not interact with AtPIP2A (C, H); OsHKT1;3 does not form oligomers (D); and the transporter and the aquaporin do not interact (F, G). (I) Oligomerization of AtPIP2A. Scale bar=25 μm.