Protocol

Whole-Mount RNA In Situ Hybridization and Immunofluorescence of Xenopus Embryos and Tadpoles

  1. Helen Rankin Willsey1
  1. Department of Psychiatry and Behavioral Sciences, Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California 94143, USA
  1. 1Correspondence: helen.willsey{at}ucsf.edu

Abstract

A major advantage of experimentation in Xenopus is the ability to query the localization of endogenous proteins and RNAs in situ in the entire animal during all of development. Here I describe three variations of staining to visualize mRNAs and proteins in developing Xenopus embryos and tadpoles. The first section outlines a traditional colorimetric staining for mRNAs that is suitable for all stages of development, and the second extends this protocol for fluorescence-based detection for higher spatial and quantitative resolution. The final section details detection of proteins by immunofluorescence, optimized for tadpole stages but widely applicable to others. Finally, optimization strategies are provided.

Footnotes

  • From the Xenopus collection, edited by Hazel L. Sive.

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  1. Cold Spring Harb Protoc © 2021 Cold Spring Harbor Laboratory Press
  1. All Versions of this Article:
    1. pdb.prot105635v1
    2. 2021/10/pdb.prot105635 most recent

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