Literature DB >> 35486237

Identification and Visualization of Protein Expression in Whole Mouse Embryos by Immunofluorescence.

V Pragathi Masamsetti1,2, Patrick P L Tam3,4.   

Abstract

Mouse embryo studies are pivotal for the understanding of early development. Analysis of the spatial and temporal changes of protein expression during development of a mouse embryo allows us to identify the genetic basis of errors of development in animal disease models. Immunofluorescence is a powerful technique to study the localization and variation in expression pattern of specific proteins in cells, tissues, and organs. Detecting the antigens with their specific antibodies labeled with fluorescent probes allows visualization of proteins at the cellular level. Here, we provide the optimized protocol of immunostaining whole mouse embryos at embryonic stages E7.5 to E11.5.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Confocal microscopy; Immunostaining; Mouse embryos; Whole mount

Mesh:

Substances:

Year:  2022        PMID: 35486237     DOI: 10.1007/978-1-0716-2281-0_4

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

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6.  TWIST1 and chromatin regulatory proteins interact to guide neural crest cell differentiation.

Authors:  Xiaochen Fan; V Pragathi Masamsetti; Jane Qj Sun; Kasper Engholm-Keller; Pierre Osteil; Joshua Studdert; Mark E Graham; Nicolas Fossat; Patrick Pl Tam
Journal:  Elife       Date:  2021-02-08       Impact factor: 8.140

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  7 in total

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