{"title":"Issue Information TOC","authors":"","doi":"10.1002/cpcy.57","DOIUrl":null,"url":null,"abstract":"<p><b>Cover</b>: In Klimas et al. (https://doi.org/10.1002/cpcy.67), Representative results from sagittal sections of mouse striatum. Pre-expanded samples were stained with DAPI (blue) and labeled for tyrosine hydroxylase (green), synaptophysin (red), and α-internexin (magenta). Pre-expansion samples are shown on the left; post-expansion on the right. (<b>A,B</b>) Successful completion resulted in a 5.27-fold expansion of the tissue from A to B. (<b>C,D</b>) Magnified images of outlined regions in A and B, respectively. (<b>E,F</b>) A separate sample that was over-homogenized shows distortion and loss of fluorescent signals for tyrosine hydroxylase and synaptophysin. All images were taken on a spinning-disk confocal microscope using a 1.1-NA 40× (<b>A-D</b>) or 0.95-NA 20× (<b>E,F</b>) water-immersion objective. Scale bars: 10 µm (<b>A,B</b>; post-expansion physical size 52.7 µm); 5 µm (<b>C,D</b>; post-expansion physical size 26.4 µm); (<b>E,F</b>) 100 µm.\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":11020,"journal":{"name":"Current Protocols in Cytometry","volume":"91 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcy.57","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cytometry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcy.57","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Health Professions","Score":null,"Total":0}
引用次数: 0
Abstract
Cover: In Klimas et al. (https://doi.org/10.1002/cpcy.67), Representative results from sagittal sections of mouse striatum. Pre-expanded samples were stained with DAPI (blue) and labeled for tyrosine hydroxylase (green), synaptophysin (red), and α-internexin (magenta). Pre-expansion samples are shown on the left; post-expansion on the right. (A,B) Successful completion resulted in a 5.27-fold expansion of the tissue from A to B. (C,D) Magnified images of outlined regions in A and B, respectively. (E,F) A separate sample that was over-homogenized shows distortion and loss of fluorescent signals for tyrosine hydroxylase and synaptophysin. All images were taken on a spinning-disk confocal microscope using a 1.1-NA 40× (A-D) or 0.95-NA 20× (E,F) water-immersion objective. Scale bars: 10 µm (A,B; post-expansion physical size 52.7 µm); 5 µm (C,D; post-expansion physical size 26.4 µm); (E,F) 100 µm.
期刊介绍:
Published in affiliation with the International Society for Advancement of Cytometry, Current Protocols in Cytometry is a "best practices" collection that distills and organizes the absolute latest techniques from the top cytometry labs and specialists worldwide. It is the most complete set of peer-reviewed protocols for flow and image cytometry available.