Cite as: Cold Spring Harb. Protoc.; 2008; doi:10.1101/pdb.prot5037

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Whole Mount RNA In Situ Hybridization on Zebrafish Embryos: Hybridization

Cecilia Moens

Division of Basic Science, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA

Corresponding author (cmoens{at}fhcrc.org)


INTRODUCTION

This protocol describes procedures for detecting gene expression in zebrafish embryos in situ using labeled RNA probes. The labels (digoxigenin or fluorescein) are detected using alkaline phosphatase-conjugated antibodies that catalyze a chromogenic reaction, producing visible blue or red products. Two-color in situ hybridization can be performed by labeling with a combination of digoxigenin- and fluorescein-labeled probes and detecting the digoxigenin and fluorescein with sequential alkaline phosphatase reactions using different chromogenic substrates. In the method described here, the fluorescein-labeled probe is detected with the red substrate, but either probe can be detected with either substrate.


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This article has been cited by other articles:


Home page
CSH ProtocolsHome page
C. Moens
Whole Mount RNA In Situ Hybridization on Zebrafish Embryos: Probe Synthesis
CSH Protocols, August 1, 2008; 2008(9): pdb.prot5036 - pdb.prot5036.
[Abstract] [Full Text]


Home page
CSH ProtocolsHome page
C. Moens
Whole Mount RNA In Situ Hybridization on Zebrafish Embryos: Mounting
CSH Protocols, August 1, 2008; 2008(9): pdb.prot5038 - pdb.prot5038.
[Abstract] [Full Text]