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. 2010 Nov 16;62(3):1255–1269. doi: 10.1093/jxb/erq354

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© 2010 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/2.5), 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. 2. — Profile of total RNA in the growing pollen tubes of hyacinth. (A) Ethidium bromide-stained gel of total RNA isolated from pollen at maturity (MP), after hydration (H), and after 1, 3, 6, 12, 24, and 36 h of in vitro germination. Well-distinguishable bands corresponding to 26S rRNA and 18S rRNA as well as to tRNA are indicated with arrows. (B) Densitometric data corresponding to the 26S rRNA (black bars), 18S rRNA (grey bars), and tRNA (white bars) from A. The values represent the average of thee replicate experiments; the error bars indicate 1 SEM.