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. 2016 Aug 9;6:31226. doi: 10.1038/srep31226

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Copyright © 2016, The Author(s)

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(a) Confocal imaging of astrocytes stained with GFAP. Scale bar is 50 μm. (b) immunoblotting and quantification of the expression level of GFAP. β-actin (right panel) is used as control for signal normalization. Lower panel: histogram plots evidencing protein fold of change over the control. Note that the expression level of GFAP was not significantly different between PDL and HTlc (n = 3). Cropped images of the entire blots are reported. However, no other specific signals were observed within the blot length.