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. 2019 Sep 2;10:3945. doi: 10.1038/s41467-019-11928-w

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — Region-specific aggregation of pathological α-syn in Syn rats. a Representative dot blot of midbrain, pontine nuclei, cortex, hippocampus and striatum homogenates from 4-month-old WT and Syn rats, immunostained with the conformation-specific α-syn antibody [MJFR-14-6-4-2], and densitometric quantification. The plot shows the levels of α-syn aggregates (expressed as % of WT). (Midbrain: 6 WT rats and 7 Syn rats, Welch’s t-test **P = 0.004; Pontine nuclei: 3 rats per genotype, Welch’s t-test P = 0.926; Cortex: 5 rats per genotype, Welch’s t-test *P = 0.030; Hippocampus: 5 rats per genotype, Mann–Whitney test **P = 0.008; Striatum: 5 rats per genotype, Welch’s t-test ***P = 0.001). The full blot and raw data are provided as a Source Data file