Number of the records: 1  

Beyond the whole-mount phenotype: high-resolution imaging in fluorescence-based applications on zebrafish

  1. 1.
    0506134 - ÚŽFG 2020 RIV GB eng J - Journal Article
    Oralová, Veronika - Rosa, J. T. - Soenens, M. - Bek, J. W. - Willaert, A. - Witten, P. E. - Huysseune, A.
    Beyond the whole-mount phenotype: high-resolution imaging in fluorescence-based applications on zebrafish.
    Biology Open. Roč. 8, č. 5 (2019), č. článku UNSP bio042374. ISSN 2046-6390. E-ISSN 2046-6390
    Institutional support: RVO:67985904
    Keywords : zebrafish * GMA * GFP * fluorophores * immunofluorescence
    OECD category: Developmental biology
    Impact factor: 2.029, year: 2019
    Method of publishing: Open access
    https://bio.biologists.org/content/8/5/bio042374

    Zebrafish is now widely used in biomedical research as a model for human diseases, but the relevance of the model depends on a rigorous analysis of the phenotypes obtained. Many zebrafish disease models, experimental techniques and manipulations take advantage of fluorescent reporter molecules. However, phenotypic analysis often does not go beyond establishing overall distribution patterns of the fluorophore in whole-mount embryos or using vibratome or paraffin sections with poor preservation of tissue architecture and limited resolution. Obtaining high-resolution data of fluorescent signals at the cellular level from internal structures mostly depends on the availability of expensive imaging technology. Here, we propose a new and easily applicable protocol for embedding and sectioning of zebrafish embryos using in-house prepared glycol methacrylate (GMA) plastic that is suited for preservation of fluorescent signals (including photoactivatable fluorophores) without the need for antibodies. Four main approaches are described, all involving imaging fluorescent signals on semithin (3 mu m or less) sections. These include sectioning transgenic animals, whole-mount immunostained embryos, cell tracking, as well as on section enzyme histochemistry.
    Permanent Link: http://hdl.handle.net/11104/0297397

     
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.