Fluorescent microscopy (76 Ergebnisse)

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Spiral Bound. Zustand: Very Good +. No Jacket. Very Good + copy. (see picture) 333 pages.All clean and tight.We also have Part B. Listed,book # 007793.

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Paperback. Zustand: Brand New. 116 pages. 9.25x6.10x0.32 inches. In Stock.

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paperback. Zustand: Gut. 333 Seiten; 9780126847543.3 Gewicht in Gramm: 1.

333 Seiten. Hardcover. Ordnungsgemäß aus einer Universitäts-Bibliothek ausgesondert (Stempel, Signatur). Sehr guter Zustand. Sprache: Englisch Gewicht in Gramm: 759.

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(S. A. Mycologia 76, 3) 1984. S. 462 - 467. m. zahlr. Abb. geklammert -2) Sonderabdruck.

Hardcover. 333 p. Good condition. The reading pages are clean and unmarked. Slight signs of storage and use. Retired library copy with corresponding labelling. Otherwise a good copy. 9780125641296 Sprache: Englisch Gewicht in Gramm: 726.

Paperback. Zustand: New. In shrink wrap. Looks like an interesting title.

Zustand: good. A copy that has been read, remains in good condition. All pages are intact, and the cover is intact. The spine and cover show signs of wear. Pages can include notes and highlighting and show signs of wear, and the copy can include "From the library of" labels or previous owner inscriptions. 100% GUARANTEE! Shipped with delivery confirmation, if you're not satisfied with purchase please return item! Ships via media mail.…

Zustand: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

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Zustand: Hervorragend. Zustand: Hervorragend | Sprache: Englisch | Produktart: Bücher | This book highlights the effectiveness of differential diagnosis in the degree of severity of joint pathology from a clinical, biophysical, and informational point of view. It includes the following information blocks:¿ Two-dimensional digital polarization microscopy of polycrystalline films of synovial fluid and determination of the coordinate distributions of the orientation and phase parameters of the microscopic image from a set of parameters of the Stokes vector.¿ Mueller-matrix mapping of polycrystalline films of synovial fluid and determination of a set of coordinate distributions (Mueller-matrix images (MMI)) of azimuthal-invariant elements that characterize manifestations of optical activity and linear birefringence.¿ Development of algorithms for polarization reproduction of distributions of linear and circular birefringence of polycrystalline films of synovial fluid.¿ Identification of digital statistical, correlation and wavelet criteria of polarization and Mueller-matrix differential diagnosis of the degree of severity of joint pathology.¿ Determination of maps of laser-induced fluorescence of synovial fluid polycrystalline films.¿ Identification of statistical and correlational criteria for fluorescent differential diagnosis of the degree of severity of joint pathology.¿ Operational characteristics of the power of the methods of azimuth-invariant polarization, Mueller-matrix and laser autofluorescence microscopy of polycrystalline films of synovial fluid.…

Gebunden. Zustand: New. Invited Review Lectures: Recent Developments in Fluorescence Microscopy Long-Lived Metal-Ligand Probes Three-Photon Excitation and Optical Control of Excited State Population J.R. Lakowicz, et al. Computer Simulations of the .

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Zustand: Used. pp. 328.

Zustand: Used. pp. 328 52:B&W 6.14 x 9.21in or 234 x 156mm (Royal 8vo) Case Laminate on White w/Gloss Lam.

Zustand: Used. pp. 328.

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Fluorescence microscopy images can be easily integrated into current video and computer image processing systems. People like visual observation; they like to watch a television or computer screen, and fluorescence techniques are thus becoming more and more popular. Since true in vivo experiments are simple to perform, samples can be directly seen and there is always the possibility of manipulating the samples during the experiments; it is an ideal technique for biology and medicine. Images are obtained by a classical (now called wide-field) fluorescence microscope, a confocal scanning microscope, upright or inverted, with epifluorescence or transmission. Computerized image processing may improve definition, and remove glare and scattered light signal. It also makes it possible to compute ratio images (ratio imaging both in excitation and in emission) or lifetime imaging. Image analysis programs may supply a great deal of additional data of various types, starting with calculations of the number of fluorescent objects, their shapes, brightness, etc. Fluorescence microscopy data may be complemented by classical measurement in the cuvette yr by flow cytometry.…

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Fluorescence microscopy images can be easily integrated into current video and computer image processing systems. People like visual observation; they like to watch a television or computer screen, and fluorescence techniques are thus becoming more and more popular. Since true in vivo experiments are simple to perform, samples can be directly seen and there is always the possibility of manipulating the samples during the experiments; it is an ideal technique for biology and medicine. Images are obtained by a classical (now called wide-field) fluorescence microscope, a confocal scanning microscope, upright or inverted, with epifluorescence or transmission. Computerized image processing may improve definition, and remove glare and scattered light signal. It also makes it possible to compute ratio images (ratio imaging both in excitation and in emission) or lifetime imaging. Image analysis programs may supply a great deal of additional data of various types, starting with calculations of the number of fluorescent objects, their shapes, brightness, etc. Fluorescence microscopy data may be complemented by classical measurement in the cuvette yr by flow cytometry.…

Zustand: New.

Taschenbuch. Zustand: Neu. Fluorescent Microscopy | Bryan Heit | Taschenbuch | xii | Englisch | 2023 | Humana | EAN 9781071620533 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.

Zustand: gut. 1989. Methods in Cell Biology ; Fluorescence Microscopy of Living Cells in Culture, Part A : Fluorescent Analogs, Labeling Cells, and Basic Microscopy ; Volume 29 In englischer Sprache. pages.