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dc.contributor.authorIoannou, Androullaen
dc.contributor.authorEleftheriou, Iroen
dc.contributor.authorLubatti, Andreaen
dc.contributor.authorCharalambous, Annaen
dc.contributor.authorSkourides, Paris A.en
dc.creatorIoannou, Androullaen
dc.creatorEleftheriou, Iroen
dc.creatorLubatti, Andreaen
dc.creatorCharalambous, Annaen
dc.creatorSkourides, Paris A.en
dc.date.accessioned2019-11-04T12:50:45Z
dc.date.available2019-11-04T12:50:45Z
dc.date.issued2012
dc.identifier.issn1110-7243
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53139
dc.description.abstractThe photostability and narrow emission spectra of nanometer-scale semiconductor crystallites (QDs) make them desirable candidates for whole-mount fluorescent in situ hybridization to detect mRNA transcripts in morphologically preserved intact embryos. We describe a method for direct QD labeling of modified oligonucleotide probes through streptavidin-biotin and antibody-mediated interactions (anti-FITC and anti-digoxigenin). To overcome permeability issues and allow QD conjugate penetration, embryos were treated with proteinase K. The use of QDs dramatically increased sensitivity of whole-mount in situ hybridization (WISH) in comparison with organic fluorophores and enabled fluorescent detection of specific transcripts within cells without the use of enzymatic amplification. Therefore, this method offers significant advantages both in terms of sensitivity, as well as resolution. Specifically, the use of QDs alleviates issues of photostability and limited brightness plaguing organic fluorophores and allows fluorescent imaging of cleared embryos. It also offers new imaging possibilities, including intracellular localization of mRNAs, simultaneous multiple-transcript detection, and visualization of mRNA expression patterns in 3D. Copyright 2012 Andriani Ioannou et al.en
dc.sourceJournal of Biomedicine and Biotechnologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84856383782&doi=10.1155%2f2012%2f627602&partnerID=40&md5=3dc82aad045a9c1c9d42291dd5212f80
dc.subjectmethodologyen
dc.subjectarticleen
dc.subjectsensitivity analysisen
dc.subjectnonhumanen
dc.subjectmetabolismen
dc.subjectfluorescence in situ hybridizationen
dc.subjectimagingen
dc.subjectantibodyen
dc.subjectAnimalsen
dc.subjectanimalen
dc.subjectanimal tissueen
dc.subjectgene expression profilingen
dc.subjectgeneticsen
dc.subjectbiotinen
dc.subjectstreptavidinen
dc.subjectmessenger RNAen
dc.subjectstainingen
dc.subjectchemistryen
dc.subjectin situ hybridizationen
dc.subjectnanoparticleen
dc.subjectNanoparticlesen
dc.subjectnanocrystalen
dc.subjectpermeabilityen
dc.subjectquantum doten
dc.subjectQuantum Dotsen
dc.subjectembryoen
dc.subjectXenopusen
dc.subjectcellular distributionen
dc.subjectRNA, Messengeren
dc.subjectprenatal developmenten
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectfluorescent dyeen
dc.subjectFluorescent Dyesen
dc.subjectdigoxigeninen
dc.subjectEndopeptidase Ken
dc.subjectfluorescence analysisen
dc.subjectoligonucleotideen
dc.subjectproteinase Ken
dc.subjectwhole mount in situ hybridizationen
dc.titleHigh-resolution whole-mount in situ hybridization using quantum dot nanocrystalsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1155/2012/627602
dc.description.volume2012
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :7</p>en
dc.source.abbreviationJ.Biomed.Biotechnol.en
dc.contributor.orcidSkourides, Paris A. [0000-0003-3502-5729]
dc.gnosis.orcid0000-0003-3502-5729


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