Literature DB >> 16807897

Quality assessment of confocal microscopy slide based systems: performance.

Robert M Zucker1.   

Abstract

BACKGROUND: All fluorescence slide-based cytometry detections systems basically include the following components: (1) an excitation light source, (2) intermediate optics, and (3) a detection device consisting of a CCD camera or a PMT. The optical principles employed is slide-based systems are similar to those of confocal microscopes (CLSM).
METHODS: The following tests evaluated confocal equipment performance: dichroic reflectivity, field illumination, lens performance, laser power output, spectral registration, axial resolution, PMT reliability, and system noise.
RESULTS: Quality assurance tests provide a basis to determine if the equipment is operating correctly. Laser power, PMTs function, dichroic reflection, spectral registration, axial registration, system noise and sensitivity, lens performance and laser stability were tested colocalization of UV and visible peaks of a bead should be less than 210 nm. Interference contrast optics decrease fluorescence resolution.
CONCLUSIONS: QA tests that assess CLSM system performance are also applicable to other slide-based systems. By utilization this type of testing approach, the subjective nature of assessing the CLSM may be eliminated. These tests serve as guidelines for other investigators to ensure that their machines are providing data that is accurate with the necessary resolution, sensitivity and precision. Copyright 2006 International Society for Analytical Cytology.

Entities:  

Mesh:

Year:  2006        PMID: 16807897     DOI: 10.1002/cyto.a.20314

Source DB:  PubMed          Journal:  Cytometry A        ISSN: 1552-4922            Impact factor:   4.355


  10 in total

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2.  Super-resolution fluorescence microscopy by stepwise optical saturation.

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Review 3.  Cytomics - importance of multimodal analysis of cell function and proliferation in oncology.

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5.  Quality assessment in light microscopy for routine use through simple tools and robust metrics.

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Journal:  J Cell Biol       Date:  2022-09-29       Impact factor: 8.077

6.  An integrated imaging approach to the study of oxidative stress generation by mitochondrial dysfunction in living cells.

Authors:  Wan-Yun Cheng; Haiyan Tong; Evan W Miller; Christopher J Chang; James Remington; Robert M Zucker; Philip A Bromberg; James M Samet; Thomas P J Hofer
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7.  ConfocalCheck--a software tool for the automated monitoring of confocal microscope performance.

Authors:  Keng Imm Hng; Dirk Dormann
Journal:  PLoS One       Date:  2013-11-05       Impact factor: 3.240

8.  Darkfield-confocal microscopy detection of nanoscale particle internalization by human lung cells.

Authors:  Eugene A Gibbs-Flournoy; Philip A Bromberg; Thomas P J Hofer; James M Samet; Robert M Zucker
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9.  Myosin concentration underlies cell size-dependent scalability of actomyosin ring constriction.

Authors:  Meredith E K Calvert; Graham D Wright; Fong Yew Leong; Keng-Hwee Chiam; Yinxiao Chen; Gregory Jedd; Mohan K Balasubramanian
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10.  IntensityCheck - The light measuring app for microscope performance checks and consistent fluorescence imaging.

Authors:  Dirk Dormann
Journal:  PLoS One       Date:  2019-03-28       Impact factor: 3.240

  10 in total

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