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. 2017 Jun 12;8:15800. doi: 10.1038/ncomms15800

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Copyright © 2017, The Author(s)

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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(a) Developmental expression patterns in mouse brain. Mouse brain extracts (10 μg of protein per lane) at the indicated ages (E, embryonic day; P, postnatal day) were analysed by immunoblotting with the indicated antibodies. Actin was monitored as a loading control. Synph represents synaptophysin. (b) Expression profiles of Lrfn proteins in the cerebral cortex and hippocampus during mouse postnatal development (W, postnatal week). Mouse tissue homogenates (5 μg of protein per lane) were analysed by immunoblotting. Actin was monitored as a loading control. Lrfn4 was not detected in the conditions we used. (a,b) Graphs indicate actin-normalized protein levels of PSD-95-binding Lrfn proteins, based on densitometric quantification of the indicated images. Maximal expression levels are adjusted to 100%. (c) Tissue distribution of Lrfn2 protein in 8-week-old mouse brain (10 μg of protein per lane). Graph indicates actin-normalized Lrfn2 protein level. Maximal expression level is adjusted to 100%. (a–c) Similar results were obtained in 2–6 independent blots except synaptophysin, GluN1, and GluN2B.