Analyzing the impact of genetic mutations on early neurogenesis of mammalian embryos in conventional mouse mutant models is laborious and time-consuming. To overcome these constraints and to fast-track the phenotypic analysis, we developed a protocol that harnesses the amenability of engineering genetic modifications in embryonic stem cells from which mid-gestation mouse chimeras and in vitro neuruloids are generated. These stem cell-based chimera and neuruloid experimental models allow phenotyping at early developmental time points of neurogenesis.
Keywords: Confocal microscopy; Embryos; Immunostaining; Neurogenesis; Stem cells.
© 2024. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.