{"title":"发布信息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":"{\"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}","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
摘要
封面:在Klimas等人(https://doi.org/10.1002/cpcy.67)中,小鼠纹状体矢状面切片的代表性结果。预膨胀样品用DAPI染色(蓝色),并标记酪氨酸羟化酶(绿色)、突触素(红色)和α-连接蛋白(品红)。膨胀前样品显示在左边;右边是扩张后。(A,B)成功完成后,组织从A扩大到B,扩大了5.27倍。(C,D)分别放大了A和B中轮廓区域的图像。(E,F)过度均质的单独样品显示酪氨酸羟化酶和突触素的荧光信号失真和丢失。所有图像均在旋转盘共聚焦显微镜上使用1.1-NA 40× (a -d)或0.95-NA 20× (E,F)水浸物镜拍摄。比例尺:10µm (A,B;膨胀后物理尺寸52.7µm);5µm (C,D;膨胀后物理尺寸26.4µm);(E,F) 100µm。
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.