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Open AccessJournal ArticleDOI

Quantitative analysis of histological staining and fluorescence using ImageJ.

Ellen C. Jensen
- 01 Mar 2013 - 
- Vol. 296, Iss: 3, pp 378-381
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TLDR
The cost effective answer for quantitative immunohistochemical analysis is ImageJ, a Java image processing and analysis program based on NIH Image for the Macintosh, developed by Wayne Rasband.
Abstract
An important objective for scientists is to statistically compare staining intensity (Fig. 1) or fluorescence (Fig. 2) for a particular marker between treatments or groups. Simply “eyeballing” an image and stating that a particular treatment or group is more densely stained or brightly fluorescent than another treatment or group is insufficient for scientific publications. Systems are available for image analysis in immunohistochemistry. However, many of these systems require expensive software and hardware attachments for acquisition, analysis, and storage of images. Therefore, an inexpensive and reliable alternative for image analysis is desirable. The cost effective answer for quantitative immunohistochemical analysis is ImageJ, developed by Wayne Rasband (http://imagej.nih.gov/ij/docs/index. html). ImageJ is a Java image processing and analysis program based on NIH Image for the Macintosh. ImageJ is available in the public domain (i.e., free). ImageJ runs on any computer that is a Java 1.5 or later virtual machine. Java runtime environments are available for free from Sun Microsystems or bundled with platform-specific installations of ImageJ (rsb.info.nih.gov/ij). Downloadable copies are available for Windows, Linux, and Mac OSX. For the evaluation of immunohistochemistry slides using ImageJ, images are captured onto the hard drive of the workstation computer. Thereafter, captured images are opened in NIH Image/ ImageJ for evaluating indices of positivity on immunohistochemistry slides, as well as fluorescence images.

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References
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Journal ArticleDOI

ImageJ for microscopy

TL;DR: The near-comprehensive range of import filters that allow easy access to image and meta-data, a broad suite processing and analysis routine, and enthusiastic support from a friendly mailing list are invaluable for all microscopy labs and facilities-not just those on a budget.
Journal ArticleDOI

An Official Research Policy Statement of the American Thoracic Society/European Respiratory Society: Standards for Quantitative Assessment of Lung Structure

TL;DR: The lung poses special challenges, some of which are outlined below and discussed in later sections: Heterogeneity of lung structure requires standardized preparation methods, and the practice of picking specific samples or sections often fails to account for regional heterogeneity, leading to biased conclusions with respect to the whole organ.
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Affordable image analysis using NIH Image/ImageJ.

TL;DR: “ImageJ” is a freely available java-based public-domain image processing and analysis program developed at the National Institutes of Health (NIH).
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A standard for calibration and shading correction of a fluorescence microscope.

TL;DR: Standardization of fluorescent images can be achieved by normalizing them to the image of a concentrated solution of a fluorophore, which can be used in clinical analysis as well as in routine laboratory practice.
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Standards for quantitative assessment of lung structure.

TL;DR: The february 15th, 2010, issue of the American Journal of Respiratory and Critical Care Medicine contains an official research policy statement on quantitative assessment of lung structure.
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Trending Questions (1)
How can image J be used to measure a specific feature of an image?

ImageJ can be used to measure staining intensity or fluorescence of a specific marker in an image by evaluating indices of positivity on immunohistochemistry slides or fluorescence images.