Literature DB >> 23931502

Proper alignment of the microscope.

Rudi Rottenfusser1.   

Abstract

The light microscope is merely the first element of an imaging system in a research facility. Such a system may include high-speed and/or high-resolution image acquisition capabilities, confocal technologies, and super-resolution methods of various types. Yet more than ever, the proverb "garbage in-garbage out" remains a fact. Image manipulations may be used to conceal a suboptimal microscope setup, but an artifact-free image can only be obtained when the microscope is optimally aligned, both mechanically and optically. Something else is often overlooked in the quest to get the best image out of the microscope: Proper sample preparation! The microscope optics can only do its job when its design criteria are matched to the specimen or vice versa. The specimen itself, the mounting medium, the cover slip, and the type of immersion medium (if applicable) are all part of the total optical makeup. To get the best results out of a microscope, understanding the functions of all of its variable components is important. Only then one knows how to optimize these components for the intended application. Different approaches might be chosen to discuss all of the microscope's components. We decided to follow the light path which starts with the light source and ends at the camera or the eyepieces. To add more transparency to this sequence, the section up to the microscope stage was called the "Illuminating Section", to be followed by the "Imaging Section" which starts with the microscope objective. After understanding the various components, we can start "working with the microscope." To get the best resolution and contrast from the microscope, the practice of "Koehler Illumination" should be understood and followed by every serious microscopist. Step-by-step instructions as well as illustrations of the beam path in an upright and inverted microscope are included in this chapter. A few practical considerations are listed in Section 3.
Copyright © 2013 Elsevier Inc. All rights reserved.

Keywords:  Aperture diaphragm; Condenser; Empty magnification; Field diaphragm; Illumination; Imaging; Infinity-correction; Koehler; Numerical aperture; Parfocal

Mesh:

Year:  2013        PMID: 23931502     DOI: 10.1016/B978-0-12-407761-4.00003-8

Source DB:  PubMed          Journal:  Methods Cell Biol        ISSN: 0091-679X            Impact factor:   1.441


  2 in total

1.  Determining absolute protein numbers by quantitative fluorescence microscopy.

Authors:  Jolien Suzanne Verdaasdonk; Josh Lawrimore; Kerry Bloom
Journal:  Methods Cell Biol       Date:  2014       Impact factor: 1.441

2.  Microgravity enhances the phenotype of Arabidopsis zigzag-1 and reduces the Wortmannin-induced vacuole fusion in root cells.

Authors:  Mengying Wang; Katherine Danz; Vanessa Ly; Marcela Rojas-Pierce
Journal:  NPJ Microgravity       Date:  2022-09-06       Impact factor: 4.970

  2 in total

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