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. 2008 Aug 13;59(13):3523–3531. doi: 10.1093/jxb/ern202

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© 2008 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. 6. — Transient expression of CFP-tagged AtRab proteins in protoplasts stably expressing the GFP-tagged marker PTS1 for peroxisome. Protoplasts from Arabidopsis leaf tissue were transformed with CFP-tagged AtRabC2a (A, B) or AtRabD1 (E–H). After 16 h from the transformation, each signal was observed by a conventional fluorescent microscope. (A, C, E, G) Signals of GFP-tagged PTS1 corresponding to the localization of peroxisomes. (B) Signals of CFP-tagged AtRabC2a, and (F) and (H) are AtRabD1. White arrows indicate peroxisomes not overlapping with signals of AtRabD1 in (H). (D) An image of a protoplast not transformed with the CFP-tagged AtRabC2a, and acquired through a filter for CFP. Bar = 10 μm.