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. 2009 Jan 6;60(2):603–614. doi: 10.1093/jxb/ern307

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© 2009 The Author(s).

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)

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Fig. 5. — Distribution of RFP–ARP3 sites in terminal (A–C) versus central (D–F) cells in the GFP-FABD2 cell line. The GFP–FABD2 signals are shown in A and D, the RFP–ARP3 signals in B and E, and the dual fluorescence in C and F, respectively. (G) Areal densities of ARP3 dots in distal (H1) or proximal (H2) halves of terminal versus central cells. Bars=20 μm. (H) Total number of ARP3 dots per cell in terminal versus central cells. The values in G and H represent in each case averages from 50 individuals collected from 32 independent transient transformations.