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Titlebook: Epiblast Stem Cells; Methods and Protocol Pierre Osteil Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license

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Establishment of Mouse Epiblast Stem Cellst stem cells as they share similar properties, such as their incapability to contribute to the formation of an embryo after injection into blastocyst. The epiblast stem cells (EpiSC) have delineated a novel status of pluripotency called “primed.” How to establish EpiSC from mouse embryo is described
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L-Proline Supplementation Drives Self-Renewing Mouse Embryonic Stem Cells to a Partially Primed Plurg from the least mature “ground state” to being “primed” to differentiate. Cells along this continuum are demarcated by differences in gene expression, X chromosome inactivation, ability to form chimeras and epigenetic marks. We have developed a protocol to differentiate “naïve” mESCs to a “partiall
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Identification and Visualization of Protein Expression in Whole Mouse Embryos by Immunofluorescence 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 antigen
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Small Interfering RNA (siRNA) Transfection in Epiblast Stem Cellsue to innate differences in cellular characteristics, the efficiency of lipid-based transfection is variable across cell types. Pluripotent cells which exist in a “primed” state such as human embryonic stem cells (hESCs) and mouse epiblast stem cells (mEpiSCs) are notorious for being refractory to l
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