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. 2011 Jun 30;39(18):8092–8104. doi: 10.1093/nar/gkr495

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© The Author(s) 2011. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 6. — Splicing of ESE depleted versions of HIPK3-T is not rescued by higher concentrations of nuclear Tra2β protein. (A) Two possible models of HIPK3-T splicing inclusion in response to Tra2β. (B) Graphs of dose responses of wild-type HIPK3-T and mutant HIPK3-T B1 and B3 to increasing concentrations of Tra2β (transfections of 300, 900 and 1500 ng of Tra2β expressing plasmid). (C) Levels of GFP-containing proteins were detected by α-GFP (left panel); Tra2β protein detected using α-Tra2β (middle panel); and α-tubulin (right panel) measured in parallel in transfected cells.