Titlebook: Handbook of Biological Confocal Microscopy; James B. Pawley Book 1990 Springer Science+Business Media New York 1990 biology.cell.developme

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Photon Detectors for Confocal Microscopy,this detector. If the scanning is rapid enough, a stable full-field image will be perceived. As a detector, however, the eye is less than perfect in reconstructing images if the scanning rate is too slow, or when the scanning is arranged so that all points in the object plane are sequentially projec

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Manipulation, Display, and Analysis of Three-Dimensional Biological Images,and hardware requirements, which must be considered for convenient data visualization and measurement. Much effort has been spent on developing a generalized display system that can also be used for model building and analysis. By model building we mean the interactive tracking of features in three-

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Systematik der Bildanalyse/Bildmuster,y the use of confocal sampling techniques. In this chapter I will discuss the fundamental considerations that limit the performance of all confocal microscopes. Though at present no commercially available equipment approaches these limits, I will describe some simple tests to help the user assess ho

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I. Vogt-Moykopf,S. Krysa,J. Schirren space into small boxes called . and assigning each a number—the pixel value or .. We do not display . position, but rather divide the . axis into perhaps 1000 parts and choose our . locations from those. Similarly, we don’t display all the imaginable pixel values, but rather divide the intensity ra

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,Indikationen für Drainierungen des Thorax,contrast at which this detail is presented, the depth through the object from which useful information can be derived, and the diameter of the useful field are all limited by the performance of the objective. All other imaging components, such as relay optics, Telan systems, tube lenses, and eyepiec

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