Miriam S. Lucas, P. Gasser, M. Günthert, J. Mercer, A. Helenius, R. Wepf
{"title":"Correlative 3D microscopy: CLSM and FIB/SEM tomography used to study cellular entry of vaccinia virus","authors":"Miriam S. Lucas, P. Gasser, M. Günthert, J. Mercer, A. Helenius, R. Wepf","doi":"10.1007/978-3-540-85228-5_181","DOIUrl":"https://doi.org/10.1007/978-3-540-85228-5_181","url":null,"abstract":"","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"62 1","pages":"361-362"},"PeriodicalIF":0.0,"publicationDate":"2008-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72767579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"High Speed Optical Sectioning Microscopy","authors":"U. Kubitscheck","doi":"10.1002/IMIC.200890054","DOIUrl":"https://doi.org/10.1002/IMIC.200890054","url":null,"abstract":"This microscopy meeting will be held on 22–23 September 2008, in Bonn, a city which is beautifully located in the Rhine valley, close to the scenic „Siebengebirge” with Germany's most often climbed mountain, the Dragon's Rock. The conference venues are the lecture halls of the Institute of Anatomy in Poppelsdorf, a part of Bonn, where most departments of the mathematical and natural sciences of the Rheinische Friedrich-Wilhelms Universitat of Bonn are located. The participants will be accommodated in hotels within walking distance to the conference site. The conference dinner will take place in the picturesque restaurant „Zur Lese” directly on the Rhine river.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"49 1","pages":"10-10"},"PeriodicalIF":0.0,"publicationDate":"2008-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86170428","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Automatic Quality Control of Cereals","authors":"P. Perner","doi":"10.1002/IMIC.200890041","DOIUrl":"https://doi.org/10.1002/IMIC.200890041","url":null,"abstract":"The increasing demands on the quality and consumption safety of grain imply, for food economy, increased expenditures for product and process supervision. Within the framework of the control of goods received and quality of the processing industries, various laboratory methods are applied at present to check the properties of the products and the observance of the standards. The control of the goods received decides whether the supplied goods will be accepted and allocated the status “healthy and customary” or whether the goods before storage in the silo have to be subjected to a special treatment in order to reduce impurities, moisture, etc. The evaluation of the quality features is especially important in order to store together grain of special quality grades or to process with regard to the desired quality grade of the final product.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"9 1","pages":"36-37"},"PeriodicalIF":0.0,"publicationDate":"2008-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85237344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Selective Harmonic Optical Microscopy","authors":"S. Chu","doi":"10.1002/IMIC.200890044","DOIUrl":"https://doi.org/10.1002/IMIC.200890044","url":null,"abstract":"SHG is an important contrast mechanism in optical examination for thick biological tissues. Fibrous proteins, such as myosin and collagen, exhibit biophotonic crystal nature and are dominant SHG harmonophores in vertebrates. Local molecule arrangements strongly affect SHG polarization behavior. Here we demonstrate to distinguish myosin-based muscle fibers from intertwined collagenous perimysium through SHG polarization selection, without complicated staining or sample/image processing required.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"71 1","pages":"43-45"},"PeriodicalIF":0.0,"publicationDate":"2008-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82917839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Rafts Properties Revealed by AFM","authors":"P. D. S. Kasas, C. Roduit, F. Lafont, G. Dietler","doi":"10.1002/IMIC.200890036","DOIUrl":"https://doi.org/10.1002/IMIC.200890036","url":null,"abstract":"We present a method based on atomic force microscopy which permits to detect and measure the mechanical properties of lipid rafts in living neurons. This technique, based on the interpretation of force distance curves, confirmed that rafts have a diameter lower than 70 nm and that they are stiffer than their surrounding membrane.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"1 1","pages":"22-24"},"PeriodicalIF":0.0,"publicationDate":"2008-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79586095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"International Conference on Nanoscience + Technology (ICN+T)","authors":"J. Stroscio, L. Whitman, Della Miller","doi":"10.1002/IMIC.200890030","DOIUrl":"https://doi.org/10.1002/IMIC.200890030","url":null,"abstract":"The 2008 International Conference on Nanoscience + Technology (ICN+T) being held from 20 – 25 July 2008, in Keystone, Colorado, will provide an international forum for discussion of the latest developments in nanoscale science and technology and recent advances in scanning probe microscopy and related techniques.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"67 1","pages":"11-11"},"PeriodicalIF":0.0,"publicationDate":"2008-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85073734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Lights, Camera, Action!","authors":"Esther Ahrent","doi":"10.1002/IMIC.200890042","DOIUrl":"https://doi.org/10.1002/IMIC.200890042","url":null,"abstract":"Understanding the vast array of diverse biochemical processes of the living cell is paramount to not only gaining an insight into the living organism as a whole, but also discovering when these cellular processes break down. Whilst innovative and specialised techniques have been instrumental for many advances in molecular biology, many questions concerning the structure and function of cells can only be answered by observing living cells. Live-cell imaging offers the power of capturing the dynamics of biological action in live cells and in real-time, something not previously available with biochemical approaches. Among the many optical tools that enable the capture of these cellular and molecular events, bio-luminescence imaging offers important opportunities. Although the concept of bio-luminescence microscopy (BLM) is not a novel one, recent advances introduced with new specialised imaging systems have made it a more realistic procedure.","PeriodicalId":100658,"journal":{"name":"Imaging & Microscopy","volume":"40 1","pages":"38-39"},"PeriodicalIF":0.0,"publicationDate":"2008-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90647291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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