Please use this identifier to cite or link to this item: https://doi.org/10.1038/nprot.2011.441
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dc.titleWhole-mount three-dimensional imaging of internally localized immunostained cells within mouse embryos
dc.contributor.authorYokomizo, T.
dc.contributor.authorYamada-Inagawa, T.
dc.contributor.authorYzaguirre, A.D.
dc.contributor.authorChen, M.J.
dc.contributor.authorSpeck, N.A.
dc.contributor.authorDzierzak, E.
dc.date.accessioned2014-11-26T10:00:23Z
dc.date.available2014-11-26T10:00:23Z
dc.date.issued2012-03
dc.identifier.citationYokomizo, T., Yamada-Inagawa, T., Yzaguirre, A.D., Chen, M.J., Speck, N.A., Dzierzak, E. (2012-03). Whole-mount three-dimensional imaging of internally localized immunostained cells within mouse embryos. Nature Protocols 7 (3) : 421-423. ScholarBank@NUS Repository. https://doi.org/10.1038/nprot.2011.441
dc.identifier.issn17542189
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/110798
dc.description.abstractWe describe a three-dimensional (3D) confocal imaging technique to characterize and enumerate rare, newly emerging hematopoietic cells located within the vasculature of whole-mount preparations of mouse embryos. However, the methodology is broadly applicable for examining the development and 3D architecture of other tissues. Previously, direct whole-mount imaging has been limited to external tissue layers owing to poor laser penetration of dense, opaque tissue. Our whole-embryo imaging method enables detailed quantitative and qualitative analysis of cells within the dorsal aorta of embryonic day (E) 10.5-11.5 embryos after the removal of only the head and body walls. In this protocol we describe the whole-mount fixation and multimarker staining procedure, the tissue transparency treatment, microscopy and the analysis of resulting images. A typical two-color staining experiment can be performed and analyzed in ∼6 d. © 2012 Nature America, Inc. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/nprot.2011.441
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1038/nprot.2011.441
dc.description.sourcetitleNature Protocols
dc.description.volume7
dc.description.issue3
dc.description.page421-423
dc.identifier.isiut000300948500001
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