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Collected tissues were fixed with 10% neutral buffered formalin (Fisher), dehydrated with 30% sucrose in PBS solution, and preserved in 70% denatured ethanol. Paraffin blocks and staining were completed by the UAB Neuroscience Molecular Detection Core. Immunohistochemical staining was performed using the same antibodies indicated above for Western blotting.
Copyright and License information: ©2018 The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
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