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Originally published as JHC exPRESS on December 23, 2007.
doi:10.1369/jhc.2007.950170
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Journal of Histochemistry and Cytochemistry
Volume 56 (4): 313-328, 2008
Copyright ©The Histochemical Society, Inc.


PERSPECTIVES

Multiple Immunoenzyme Staining: Methods and Visualizations for the Observation With Spectral Imaging

Chris M. van der Loos

Department of Pathology, Academic Medical Center, Amsterdam, The Netherlands

Correspondence to: Chris M. van der Loos, PhD, Department of Pathology, Academic Medical Center, M2-230 Meibergdreef 9, NL-1105 AZ Amsterdam, The Netherlands. E-mail: c.m.vanderloos{at}amc.uva.nl

Summary

Several staining concepts and color combinations exist to perform successful double immunoenzyme staining on human tissue specimens. Most of these concepts are based on differences between both primary antibodies: animal species, mouse Ig isotype or IgG subclasses, conjugates, or concentrations. Traditionally, double immunoenzyme staining has used chromogens selected to provide maximum color contrast when observed with the unaided eye. Unfortunately, visually good color combinations always include at least one diffuse chromogen, because of the paucity of appropriate chromogen colors. This situation is drastically changed with the use of spectral imaging, where multicolor microscopy can be unmixed in individual images based on their spectral characteristics. Spectral unmixing can be performed even up to quadruple immunoenzyme staining. This work contains practical suggestions for immunoenzyme double staining procedures for some frequently encountered primary antibody combinations: rabbit–mouse, goat–mouse, mouse–mouse, and rabbit–rabbit. The suggested protocols are all suitable for a classical red-brown color combination plus blue nuclear counterstain that is composed of peroxidase activity (diaminobenzidine tetrahydrochloride), alkaline phosphatase activity (Liquid Permanent Red), and hematoxylin, respectively. Although the red and brown chromogens do not contrast very well visually, they both show a crisp localization and can be perfectly unmixed by spectral imaging. (J Histochem Cytochem 56:313–328, 2008)

Key Words: immuno-double staining • immuno-quadruple staining • chromogens • spectral imaging • unmixing


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