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An Improved Method for Three-dimensional Reconstruction of Protein Expression Patterns in Intact Mouse and Chicken Embryos and Organs
Author(s) -
Jonas Ahnfelt-Ro̷nne,
Mette C. Jørgensen,
Jacob Hald,
Ole Madsen,
Palle Serup,
Jacob HecksherSørensen
Publication year - 2007
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/jhc.7a7226.2007
Subject(s) - confocal , software , embryo , microscope , confocal microscopy , immunofluorescence , protocol (science) , computer science , resolution (logic) , biology , fish <actinopterygii> , microbiology and biotechnology , computational biology , artificial intelligence , optics , antibody , physics , pathology , genetics , medicine , alternative medicine , programming language , fishery
We have developed a wholemount immunofluorescence protocol for the simultaneous detection of up to three proteins in mouse and chicken embryos. Combined with Murray's clearing reagent (BABB) and microscope objectives with long working ranges and high numerical apertures mounted on a confocal microscope, cellular resolution can be obtained in depths offering the possibility of examining expression patterns in entire organs or embryos. Three-dimensional projections of the optical confocal sections can be computed with computer software allowing rotation around any axis. The protocol is robust and we find that most antibodies working on tissue sections also work with this protocol. This manuscript contains online supplemental material at http://www.jhc.org. Please visit this article online to view these materials.

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