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. 2008 Dec 10;60(1):169–185. doi: 10.1093/jxb/ern273

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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.

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Fig. 2. — Histochemical localization of GUS activity in transgenic tomato plants under control of the AGPL1 and CaMV 35S promoters. Transgenic tomato carrying the AGPL1 promoter fused to GUS (A–E): (A) leaf; (B) root; (C) longitudinal section of stem; (D) transverse section of stem; (E) fruit. Transgenic tomato carrying the CaMV 35S promoter fused to GUS (a–e): (a) leaf; (b) root; (c) longitudinal section of stem; (d) transverse section of stem; (dd) bud; (e) fruit. (E and e) Note that the driving patterns for the AGPL1 promoter and CaMV 35S promoter plants are different. (F) Histochemical staining of 10-d-old transgenic tomato seedlings. (This figure is available in colour at JXB online.)