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  2. Production of Digoxigenin-Labeled Riboprobes for In Situ Hybridization Experiments

Production of Digoxigenin-Labeled Riboprobes for In Situ Hybridization Experiments

  • Curr Protoc Mouse Biol. 2020 Jun;10(2):e74. doi: 10.1002/cpmo.74.
Kristen S Barratt 1 Ruth M Arkell 1
Affiliations

Affiliation

  • 1 Early Mammalian Development Laboratory, John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Abstract

Experiments that visualize gene expression in intact tissues or organisms are fundamental to studies of gene function. These experiments, called in situ hybridization, require the production of a riboprobe, which is a labeled antisense RNA corresponding to a particular gene. The most commonly used system for visualizing gene expression via in situ hybridization is the incorporation of a digoxigenin label into an in vitro-transcribed RNA probe. After hybridization of the riboprobe to a target mRNA, its location can be detected via a high-affinity α-digoxigenin antibody conjugated to an alkaline-phosphatase Enzyme. The article describes the design and production of digoxigenin-labeled riboprobes transcribed in vitro from template DNA (either plasmid or PCR amplicon). These riboprobes are suitable for use in tissue and whole-mount in situ hybridization protocols. © 2020 by John Wiley & Sons, Inc. Basic Protocol 1: Plasmid-derived riboprobes Alternate Protocol: PCR-derived riboprobes Basic Protocol 2: Riboprobe synthesis with DIG label.

Keywords

RNA detection; digoxigenin; fluorescein; gene expression; hybridization; mouse embryo; riboprobe.

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