{"title":"用共聚焦荧光显微镜成像活细胞中的线粒体","authors":"T. Peng, M. Jou","doi":"10.1109/APBP.2004.1412293","DOIUrl":null,"url":null,"abstract":"Images of mitochondria inside living cells with high spatial and temporal resolution could be visualized with specific functional fluorescent probes coupled with laser scanning confocal microscope. The interactions between mitochondria and other parts of cells remain nature and unaltered with this method. The effects of mitochondrial function changes on other parts of cells can best be investigated with this approach.","PeriodicalId":346624,"journal":{"name":"The Second Asian and Pacific Rim Symposium on Biophotonics, 2004. APBP 2004.","volume":"14 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2004-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Imaging mitochondria in living cells by confocal fluorescence microscopy\",\"authors\":\"T. Peng, M. Jou\",\"doi\":\"10.1109/APBP.2004.1412293\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Images of mitochondria inside living cells with high spatial and temporal resolution could be visualized with specific functional fluorescent probes coupled with laser scanning confocal microscope. The interactions between mitochondria and other parts of cells remain nature and unaltered with this method. The effects of mitochondrial function changes on other parts of cells can best be investigated with this approach.\",\"PeriodicalId\":346624,\"journal\":{\"name\":\"The Second Asian and Pacific Rim Symposium on Biophotonics, 2004. APBP 2004.\",\"volume\":\"14 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2004-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Second Asian and Pacific Rim Symposium on Biophotonics, 2004. APBP 2004.\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/APBP.2004.1412293\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Second Asian and Pacific Rim Symposium on Biophotonics, 2004. APBP 2004.","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/APBP.2004.1412293","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Imaging mitochondria in living cells by confocal fluorescence microscopy
Images of mitochondria inside living cells with high spatial and temporal resolution could be visualized with specific functional fluorescent probes coupled with laser scanning confocal microscope. The interactions between mitochondria and other parts of cells remain nature and unaltered with this method. The effects of mitochondrial function changes on other parts of cells can best be investigated with this approach.
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