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Human Molecular Genetics 2006 15(4):665; doi:10.1093/hmg/ddi488
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© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

CORRIGENDUM

Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REG{gamma} as a therapeutic target

John S. Bett, Geoffrey M. Goellner, Ben Woodman, Gregory Pratt, Martin Rechsteiner and Gillian P. Bates

Human Molecular Genetics (2006) 15, 33–44; doi:10.1093/hmg/ddi423

This figure has been reproduced as a corrigendum because the upper and lower panels of Figure 2B were blank in the original publication of this paper.


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Figure 2. REG{gamma} is highly expressed in the mouse brain and is restricted to neuronal nuclei. (A) Coronal sections through cortex of WT and REG{gamma} null mouse brain reveal a predominant nuclear localization of REG{gamma}. The absence of any specific staining in the null mice confirms that REG{gamma} has been successfully knocked out and that the antibody is specific. Arrow points to a nucleus expressing REG{gamma}, and inset shows higher magnification of another nucleus expressing REG{gamma}. The nuclear counterstain is methyl green. (B) Western blot analysis on nuclear and cytoplasmic 12-week-old brain fractions confirms that REG{gamma} has a nuclear localizati on. Blots were stained with histone H2B as a nuclear marker and ß-actin as a cytoplasmic marker. (C) REG{gamma} colocalizes with the neuronal marker NeuN in the mouse brain. No REG{gamma} was detected in glial cells. Ctx, cortex; cyt, cytoplasm and nuc, nucleus.

 

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