{"title":"共焦显微镜","authors":"S. Cody, G. Cox","doi":"10.1201/9781351129404-3","DOIUrl":null,"url":null,"abstract":"\"We are now able to take a series of photographs at slightly different focal planes or levels through a single cell or group of cells. These photographs result in a consecutive record of the internal architecture of the cell or cells. This accomplishment we have called \"optical sectioning\". ... By means of this new development a transparent specimen such as a group of cells may be sectioned optically. ... Detail above or below the focal plane does not interfere.\" [1]","PeriodicalId":394303,"journal":{"name":"Fundamentals of Fluorescence Imaging","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Confocal Microscopy\",\"authors\":\"S. Cody, G. Cox\",\"doi\":\"10.1201/9781351129404-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\\"We are now able to take a series of photographs at slightly different focal planes or levels through a single cell or group of cells. These photographs result in a consecutive record of the internal architecture of the cell or cells. This accomplishment we have called \\\"optical sectioning\\\". ... By means of this new development a transparent specimen such as a group of cells may be sectioned optically. ... Detail above or below the focal plane does not interfere.\\\" [1]\",\"PeriodicalId\":394303,\"journal\":{\"name\":\"Fundamentals of Fluorescence Imaging\",\"volume\":\"45 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fundamentals of Fluorescence Imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1201/9781351129404-3\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fundamentals of Fluorescence Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1201/9781351129404-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
"We are now able to take a series of photographs at slightly different focal planes or levels through a single cell or group of cells. These photographs result in a consecutive record of the internal architecture of the cell or cells. This accomplishment we have called "optical sectioning". ... By means of this new development a transparent specimen such as a group of cells may be sectioned optically. ... Detail above or below the focal plane does not interfere." [1]
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