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dc.contributor.authorRentzsch, Fabian
dc.contributor.authorRenfer, Eduard
dc.contributor.authorTechnau, Ulrich
dc.date.accessioned2021-05-07T12:08:09Z
dc.date.available2021-05-07T12:08:09Z
dc.date.created2020-08-13T13:09:59Z
dc.date.issued2020
dc.PublishedMethods in molecular biology. 2020, 2047 45-57.
dc.identifier.issn1064-3745
dc.identifier.urihttps://hdl.handle.net/11250/2754173
dc.description.abstractNeurons often display complex morphologies with long and fine processes that can be difficult to visualize, in particular in living animals. Transgenic reporter lines in which fluorescent proteins are expressed in defined populations of neurons are important tools that can overcome these difficulties. By using membrane-attached fluorescent proteins, such reporter transgenes can identify the complete outline of subsets of neurons or they can highlight the subcellular localization of fusion proteins, for example at pre- or postsynaptic sites. The relative stability of fluorescent proteins furthermore allows the tracing of the progeny of cells over time and can therefore provide information about potential roles of the gene whose regulatory elements are controlling the expression of the fluorescent protein. Here we describe the generation of transgenic reporter lines in the sea anemone Nematostella vectensis, a cnidarian model organism for studying the evolution of developmental processes. We also provide an overview of existing transgenic Nematostella lines that have been used to study conserved and derived aspects of nervous system development.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.titleGenerating transgenic reporter lines for studying nervous system development in the cnidarian nematostella vectensisen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright 2020 Springer Science+Business Media, LLCen_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.doi10.1007/978-1-4939-9732-9_3
dc.identifier.cristin1823167
dc.source.journalMethods in molecular biologyen_US
dc.source.402047
dc.source.pagenumber45-57en_US
dc.identifier.citationMethods in molecular biology. 2020, 2047, 45-57en_US
dc.source.volume2047en_US


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