Whole-Mount In Situ Hybridization in Post-Implantation Staged Mouse Embryos
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Barratt, Kristen
Arkell, Ruth
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John Wiley & Sons, Inc.
Abstract
Understanding RNA expression in space and time is a key initial step in dissecting gene function. The ability to visualize gene expression in whole-tissue
or whole-specimen preparations, called in situ hybridization (ISH), was first
developed 50 years ago. Two decades later, these protocols were adapted to
establish robust methods for whole-mount ISH to murine embryos. The precise
protocols vary somewhat between early-gestation and mid-gestation mouse
embryos; the protocol presented here is optimal for use with post-implantation
stage mouse embryos (stages 5.5–9.5 dpc). Routine uses of whole-mount ISH
include documenting the wild-type expression pattern of individual genes
and comparison of the expression pattern of signature genes (i.e., those that
identify particular cells and tissues within an embryo) between wild-type and
mutant embryos as part of a phenotyping experiment. This technique remains
a mainstay of developmental biology studies and complements the massively
parallel assessment of gene expression from dissociated tissues and cells via
RNA-sequencing techniques
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Current Protocols in Mouse Biology
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Restricted until
2099-12-31
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