{"title":"用于检测荧光标记单分子的附微流控TIRF显微镜的建立","authors":"Anxiong Yang, R. Börner","doi":"10.52825/ocp.v2i.140","DOIUrl":null,"url":null,"abstract":"At Laserinstitut Hochschule Mittweida (LHM), single molecule fluorescence microscopy is to be established for biophotonic RNA research. The aim of this work is to establish an objective-based total internal reflection fluorescence microscope (TIRFM) with alternating laser excitation (ALEX) in the millisecond range. We have designed a suitable detection beam path for color channel-selected imaging with a scientific CMOS camera. The two detection channels allow distance changes to be measured at the molecular level using Förster resonance energy transfer (FRET). In addition to the microscope setup, this work details the imaging and color channel selection of the fluorescently labeled samples and the modulated laser excitation.","PeriodicalId":89291,"journal":{"name":"The open conference proceedings journal","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Setup of a TIRF Microscope With Attached Microfluidics for the Detection of Fluorescently Labeled Single Molecules\",\"authors\":\"Anxiong Yang, R. Börner\",\"doi\":\"10.52825/ocp.v2i.140\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"At Laserinstitut Hochschule Mittweida (LHM), single molecule fluorescence microscopy is to be established for biophotonic RNA research. The aim of this work is to establish an objective-based total internal reflection fluorescence microscope (TIRFM) with alternating laser excitation (ALEX) in the millisecond range. We have designed a suitable detection beam path for color channel-selected imaging with a scientific CMOS camera. The two detection channels allow distance changes to be measured at the molecular level using Förster resonance energy transfer (FRET). In addition to the microscope setup, this work details the imaging and color channel selection of the fluorescently labeled samples and the modulated laser excitation.\",\"PeriodicalId\":89291,\"journal\":{\"name\":\"The open conference proceedings journal\",\"volume\":\"26 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The open conference proceedings journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.52825/ocp.v2i.140\",\"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 open conference proceedings journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52825/ocp.v2i.140","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Setup of a TIRF Microscope With Attached Microfluidics for the Detection of Fluorescently Labeled Single Molecules
At Laserinstitut Hochschule Mittweida (LHM), single molecule fluorescence microscopy is to be established for biophotonic RNA research. The aim of this work is to establish an objective-based total internal reflection fluorescence microscope (TIRFM) with alternating laser excitation (ALEX) in the millisecond range. We have designed a suitable detection beam path for color channel-selected imaging with a scientific CMOS camera. The two detection channels allow distance changes to be measured at the molecular level using Förster resonance energy transfer (FRET). In addition to the microscope setup, this work details the imaging and color channel selection of the fluorescently labeled samples and the modulated laser excitation.