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. 2018 Jul 25;15:213. doi: 10.1186/s12974-018-1255-9

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© The Author(s). 2018

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. 2 — Characterization of CSF-ADAM10 complexes by sucrose gradient ultracentrifugation. CSF samples (NADC) were fractionated on 5–20% sucrose density gradients. The fractions (collected from the top of each tube) were immunoblotted using the ectodomain antibody specific for a domain common to all the soluble CSF-ADAM10 species. Enzymes of known sedimentation coefficient, alkaline phosphatase (P, 6.1S; ~ 140–160 kDa), catalase (C, 11.4S; ~ 232 kDa), and β-galactosidase (G, 16.0S; ~ 540 kDa) were used as internal markers. A representative case from three independent experiments is shown