Last edited by Mokinos
Saturday, May 9, 2020 | History

3 edition of Three-dimensional microscopy found in the catalog.

Three-dimensional microscopy

image acquisition and processing : 7-8 February 1994, San Jose, California

  • 124 Want to read
  • 22 Currently reading

Published by SPIE in Bellingham, Wash., USA .
Written in English

    Subjects:
  • Confocal microscopy -- Congresses.,
  • Fluorescence microscopy -- Congresses.,
  • Image processing -- Congresses.,
  • Three-dimensional imaging in biology -- Congresses.

  • Edition Notes

    Includes bibliographical references and author index.

    StatementCarol J. Cogswell, Kjell Carlsson, chairs/editors ; sponsored by IS&T--the Society for Imaging Science and Technology, SPIE--the International Society for Optical Engineering.
    SeriesProceedings / SPIE--the International Society for Optical Engineering ;, v. 2184, Proceedings of SPIE--the International Society for Optical Engineering ;, v. 2184.
    ContributionsCogswell, Carol J., Carlsson, Kjell., IS & T--the Society for Imaging Science and Technology., Society of Photo-optical Instrumentation Engineers.
    Classifications
    LC ClassificationsQH224 .T47 1994
    The Physical Object
    Paginationix, 270 p. :
    Number of Pages270
    ID Numbers
    Open LibraryOL1447583M
    ISBN 100819414794
    LC Control Number93087319
    OCLC/WorldCa30307193

    Three-dimensional confocal microscopy of colloids A. D. Dinsmore, Eric R. Weeks, Vikram Prasad, Andrew C. Levitt, and D. A. Weitz Confocal microscopy is used in the study of colloidal gels. Structured Light for Three-Dimensional Microscopy Leo G. Krzewina ABSTRACT The conventional light microscope is an indispensable tool for many physical and life science applications, but is of limited usefulness for three-dimensional imaging due to its increasingly narrow depth of field at high magnifications. Focused regions may be.

    Read "Three-Dimensional Electron Microscopy of Macromolecular Assemblies Visualization of Biological Molecules in Their Native State" by Joachim Frank available from Rakuten Kobo. Cryoelectron microscopy of biological molecules is among the hottest growth areas in biophysics and structural biology aBrand: Oxford University Press.   Abstract. Locating a molecule within a cell using protein-tagging and immunofluorescence is a fundamental technique in cell biology, whereas in three-dimensional electron microscopy, locating a subunit within a macromolecular complex remains by: 3.

    This book highlights the unity of electron microscopy, X-ray microscopy and optical microscopy: diffraction, aberrations, three-dimensional reconstruction algorithms, Fourier optics, detectors and contrast mechanisms across various modalities of microscopy. In transmission microscopy, many objects are three dimensional, that is, they are thicker than the depth of focus of the imaging system. The three-dimensional (3-D) image-intensity distribution consists of a series of two-dimensional images (optical slices) with different parts of the object in focus. First, we deal with the fundamental limitations of 3-D imaging with classical optical systems.


Share this book
You might also like
ideal and the real

ideal and the real

Feasibility study for a generalized gate logic software simulator

Feasibility study for a generalized gate logic software simulator

And Schumpeter said, this is how thou shalt grow

And Schumpeter said, this is how thou shalt grow

Long-term growth of eight legumes introduced at three forest locations in southwest Oregon

Long-term growth of eight legumes introduced at three forest locations in southwest Oregon

Randomization and the limit points of monopolistic competition

Randomization and the limit points of monopolistic competition

Good Practices to Protect Women Migrant Wokers in Countries of Employment

Good Practices to Protect Women Migrant Wokers in Countries of Employment

San Antonio Missions National Historical Park

San Antonio Missions National Historical Park

assessment of middle-management volunteers in Oregons 4-H programs

assessment of middle-management volunteers in Oregons 4-H programs

climate near the ground

climate near the ground

The Slater Creed

The Slater Creed

The Missouri Gardeners Companion

The Missouri Gardeners Companion

Talks to Teachers

Talks to Teachers

life, character and times of Oliver Cromwell

life, character and times of Oliver Cromwell

Little Number Stories

Little Number Stories

Three-dimensional microscopy Download PDF EPUB FB2

Three-Dimensional Electron Microscopy of Macromolecular Assemblies is the first systematic introduction to single-particle methods of reconstruction. It covers correlation alignment, classification, 3D reconstruction, restoration, and interpretation of the resulting 3D images in macromolecular assemblies.

Three-Dimensional Electron Microscopy. Edited by Thomas Müller-Reichert, Gaia Pigino. VolumePages () Serial-section electron microscopy using automated tape-collecting ultramicrotome (ATUM) Book chapter Full text access.

Three-Dimensional Electron Microscopy of Macromolecular Assemblies: Visualization of Biological Molecules in Their Native State 2nd Edition by Joachim Frank (Author) out of 5 stars 3 ratings.

ISBN ISBN Why is ISBN important. ISBN. This bar-code number lets you verify that you're getting exactly the right Cited by: About this book.

This book is on three-dimensional electron microscopy (sometime referred to as 3DEM) that includes both cryo-electron microscopy and cyro-electron tomography. The goal of this book is to take all of the material on 3DEM and put it into an organized form.

This organized book can then in turn be used for training new scientists in the field, teaching a course on 3DEM, or just. Computational Methods for Three-Dimensional Microscopy Reconstruction will serve as a useful resource for scholars interested in the development of computational methods for structural biology and cell biology, particularly in the area of 3D imaging and modeling.

Product : Hardcover. Purchase Three-Dimensional Electron Microscopy, Volume - 1st Edition. Print Book & E-Book. ISBN  Cryoelectron microscopy of biological molecules is among the hottest growth areas in biophysics and structural biology at present, and Frank is arguably the most distinguished practitioner of this art.

CryoEM is likely over the next few years to take over much of the structural approaches currently requiring X-ray crystallography, because one can now get good and finely detailed images of. The electrons will either bounce off or pass through the sample and an image will be collected depending on the type of microscopy being utilized.

The resolution capability of an electron microscope is much greater than that of a light microscope, generally obtaining a magnification of ,X which is 50,X greater than a traditional light. Three-dimensional microscopy can be used to reveal the shape, distribution, and connectivity of three-dimensional (3D) features that lie buried within an opaque material.

This article discusses several experimental techniques that can be used to generate 3D images. ISBN: OCLC Number: Description: xii, pages: color illustrations ; 25 cm.

Contents: Chapter 1. FIB-SEM of mouse nervous tissue: Fast and slow sample preparation / Anna M. Steyer, Andreas Schertel, Christos Nardis, Wiebke Möbius --Chapter ted large-volume 3-D SEM workflows for comparative microanatomical imaging / Gerald John Shami.

The book employs advanced mathematical treatments to describe three-dimensional Fourier optical principles, point spread functions, and transfer functions. Chapters include brightfield microscopy with a finite-sized detector, confocal fluorescence, two-photon, fiber optics, short pulse laser microscopy, high numerical aperture objectives, and.

Three-Dimensional Electron Microscopy, Volume in the Methods in Cell Biology series, highlights new advances in the field, with this new volume presenting interesting chapters focusing on FIB-SEM of mouse nervous tissue: fast and slow sample preparation, Serial-section electron microscopy using ATUM - Automated Tape collecting Ultra-Microtome, Software for automated acquisition of electron.

Paperback. Published: 02 February Pages | halftones & line illus. /8 x /4 inches. ISBN: Three-dimensional x-ray diffraction (3DXRD) microscopy is a novel experimental method for structural characterisation of polycrystalline materials. The position, morphology, phase, strain and crystallographic orientation of hundreds of grains or sub-grain embedded within mm-cm thick specimens can be determined simultaneously.

Microscopy is the technical field of using microscopes to view objects and areas of objects that cannot be seen with the naked eye (objects that are not within the resolution range of the normal eye). There are three well-known branches of microscopy: optical, electron, and scanning probe microscopy, along with the emerging field of X-ray microscopy.

Three-dimensional x-ray diffraction (3DXRD) microscopy is a novel experimental method for structural characterisation of polycrystalline materials. The position, morphology, phase, strain and crystallographic orientation of hundreds of grains or sub-grain embedded within mm-cm thick specimens can be determined : Springer-Verlag Berlin Heidelberg.

This book discusses the various principles in confocal scanning microscopy which has become a useful tool in many practical fields including biological studies and industrial inspection. The methodology presented in this book is unique and is based on the concept of the three-dimensional transfer functions which have been developed by the.

Borrett, S. & Hughes, L. () Reporting methods for processing and analysis of data from serial block face scanning electron microscopy. Journal of microscopy, –9. Denk, W. & Horstmann, H. () Serial block-face scanning electron microscopy to reconstruct three-dimensional tissue nanostructure.

PLoS biology, 2:eAuthor: ZEISS Microscopy. Get this from a library. Computational methods for three-dimensional microscopy reconstruction. [Gabor T Herman; J Frank;] -- Approaches to the recovery of three-dimensional information on a biological object, which are often formulated or implemented initially in an.

Three-dimensional fluorescence imaging is most commonly performed using confocal or multi-photon microscopy, the axial resolution of which is typically in the range of - nm, two to three times worse than the lateral resolution (11, 12). The axial imaging resolution can be improved to roughly nm by 4Pi and I 5 M microscopy ().

Hardcover. Published: 02 February Pages | halftones & line illus. /8 x /4 inches. ISBN: About this book Introduction Both three-dimensional electron microscopy and X-ray tomography can be captured in the same mathematical framework, leading to closely-related computational approaches, but the methodologies differ in detail and hence pose different challenges.Unbiased Stereology Three Dimensional Measurement in Microscopy C.V.

Howard & M.G. Reed This book is a simple and practical guide to making unbiased 3-D measurements of microstructure via the microscope. It is not full of complex mathematics and is of use to biologists, toxicologists, pathologists, geologists and materials scientists.