Literature DB >> 14719342

Ratio imaging instrumentation.

Kenneth Dunn1, Frederick R Maxfield.   

Abstract

Using ratio imaging to obtain quantitative information from microscope images is a powerful tool that has been used successfully in numerous studies. Although ratio imaging reduces the effects of many parameters that can interfere with accurate measurements, it is not a panacea. In designing a ratio imaging experiment, all of the potential problems discussed in this chapter must be considered. Undoubtedly, other problems that were not discussed can also interfere with accurate and meaningful measurements. Many of the problems discussed here were observed in the authors' laboratories. In our experience there are no standard routines or methods that can foresee every problem before it has been encountered. Good experimental design can minimize problems, but the investigator must continue to be alert. Progress in instrumentation continues to overcome some of the difficulties encountered in ratio imaging. CCD cameras with 12- to 14-bit pixel depth are being used more frequently, and several confocal microscope manufacturers are now also using 12-bit digitization. The dramatic increase in the use of confocal microscopes over the past decade is now causing microscope manufacturers to more critically evaluate the effect of axial chromatic aberration in objectives, and recent designs to minimize this problem are being implemented. Other developments such as the use of AOTFs to attenuate laser lines extend the applicability of ratio imaging. Ratio imaging is clearly applicable to a wide range of cell biological problems beyond its widespread use for measuring ion concentrations. Imaginative but careful use of this technique should continue to provide novel insights into the properties of cells.

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Year:  2003        PMID: 14719342     DOI: 10.1016/s0091-679x(03)72019-6

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


  7 in total

1.  Noise-induced systematic errors in ratio imaging: serious artefacts and correction with multi-resolution denoising.

Authors:  Yu-Li Wang
Journal:  J Microsc       Date:  2007-11       Impact factor: 1.758

2.  The calcium channel mucolipin-3 is a novel regulator of trafficking along the endosomal pathway.

Authors:  Jose A Martina; Benjamin Lelouvier; Rosa Puertollano
Journal:  Traffic       Date:  2009-04-29       Impact factor: 6.215

3.  Apoptotic β-cells induce macrophage reprogramming under diabetic conditions.

Authors:  Meliza G Ward; Ge Li; Mingming Hao
Journal:  J Biol Chem       Date:  2018-09-13       Impact factor: 5.157

4.  Plasma membrane sterol distribution resembles the surface topography of living cells.

Authors:  Daniel Wüstner
Journal:  Mol Biol Cell       Date:  2006-10-25       Impact factor: 4.138

5.  Mucolipin-3 regulates luminal calcium, acidification, and membrane fusion in the endosomal pathway.

Authors:  Benjamin Lelouvier; Rosa Puertollano
Journal:  J Biol Chem       Date:  2011-01-18       Impact factor: 5.157

6.  Activation of microglia acidifies lysosomes and leads to degradation of Alzheimer amyloid fibrils.

Authors:  Amitabha Majumdar; Dana Cruz; Nikiya Asamoah; Adina Buxbaum; Istvan Sohar; Peter Lobel; Frederick R Maxfield
Journal:  Mol Biol Cell       Date:  2007-02-21       Impact factor: 4.138

7.  Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles.

Authors:  Li Ma; Qing Ouyang; Gordon C Werthmann; Heather M Thompson; Eric M Morrow
Journal:  Front Cell Dev Biol       Date:  2017-08-21
  7 in total

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