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. 2009 Aug 11;37(19):e126. doi: 10.1093/nar/gkp626

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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.

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Figure 4. — PASP of α-tropomyosin in Xenopus embryos and organs. RNAs were extracted from oocytes, stage 8 or 35 embryos, dissected embryonic somites or the indicated adult organs, and α-tropomyosin-splicing patterns were analysed by PASP. The percentages of exon 6B (mean ± SD of six independent RNA preparations) are shown (upper panel). Adult heart, oviduct stomach, and oocyte RNA were also analysed by radioactive RT–PCR as in Figure 2B (lower panel). The percentages of 6B exon (restricted by BstNI) are indicated under the gel.