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. 2016 Oct 10;4:110. doi: 10.1186/s40478-016-0381-9

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 8 — Production of murine-Aβ in H-Aβ24 and H-Aβ24/H-Aβ42 injected mice. Tris-Tricine SDS–polyacrylamide gel electrophoresis (PAGE) followed by immunoblotting using murine-Aβ-specific monoclonal antibody m3.2 of brain homogenate factions (supernatant, top panel and pellet, bottom panel) of mice injected with vehicle, H-Aβ24, H-Aβ42 or H-Aβ24/H-Aβ42 mix and analyzed after 4 months. Asterisks indicate the presence of 6KDa band positive to m3.2 antibody only in the pellet fraction of mice injected with H-Aβ24. Actin was used as loading control