Literature DB >> 2709408

A confocal laser microscope scanner for digital recording of optical serial sections.

K Carlsson1, A Liljeborg.   

Abstract

A confocal laser microscope scanner developed at our institute is described. Since an ordinary microscope is used, it is easy to view the specimen prior to scanning. Confocal imaging is obtained by laser spot illuminatin, and by focusing the reflected or fluorescent light from the specimen onto a pinhole aperture in front of the detector (a photomultiplier tube). Two rotating mirrors are used to scan the laser beam in a raster pattern. The scanner is controlled by a microprocessor which coordinated scanning, data display, and data transfer to a host computer equipped with an array processor. Digital images with up to 1024x1024 pixels and 256 grey levels can be recorded. The optical sectioning property of confocal scanning is used to record thin (about 1 microm) sections of a specimen without the need for mechanical sectioning. By using computer-control to adjust the focus of the microscope, a stack of consecutive sections can be automatically recorded. A computer is then used to display the 3-D structure of the specimen. It is also possible to obtain quantitative information, both geometric and photometric. In addition to confocal laser scanning, it is easy to perform non-confocal laser scanning, or to use conventional microscopic illumination techniques for (non-confocal) scanning. The design has proved reliable and stable, requiring very few adjustments and realignments. Results obtained with this scanner are reported, and some limitations of the technique are discussed.

Mesh:

Year:  1989        PMID: 2709408     DOI: 10.1111/j.1365-2818.1989.tb00557.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  4 in total

1.  Channel structures in aerobic biofilms of fixed-film reactors treating contaminated groundwater.

Authors:  A A Massol-Deyá; J Whallon; R F Hickey; J M Tiedje
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

2.  A confocal scanning laser microscope for quantitative ratiometric 3D measurements of [Ca2+] and Ca2+ diffusions in living cells stained with Fura-2.

Authors:  P J Helm; O Franksson; K Carlsson
Journal:  Pflugers Arch       Date:  1995-03       Impact factor: 3.657

3.  Uptake and localisation of O-(beta-hydroxyethyl)-rutosides in the venous wall, measured by laser scanning microscopy.

Authors:  H A Neumann; K Carlsson; G H Brom
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

4.  Optical sectioning of microbial biofilms.

Authors:  J R Lawrence; D R Korber; B D Hoyle; J W Costerton; D E Caldwell
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

  4 in total

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