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Automated in vivo imaging of cell interior using fluorescent proteins

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14330%2F04%3A00010822" target="_blank" >RIV/00216224:14330/04:00010822 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Automated in vivo imaging of cell interior using fluorescent proteins

  • Original language description

    Techniques with fluorescent proteins have become very valuable tools for the study of cellular processes in living cells. These proteins enable the non-invasive quantitative visualization in vivo as molecular tags on natively non-fluorescent molecules ofinterest. Fluorescent proteins are welcome innovation in the field of cell biology, because in vivo experiments bring new interesting results and different point of view than in vitro and in situ experiments. This presentation will address automated 2D/3D high-resolution confocal image acquisition and analysis of cells stained with fluorescent proteins. While the approaches to automated in situ imaging of cell interior have been previously described by our group (Cytometry 45, 1-12, 2001), this contribution will concentrate on the modifications (both hardware and software ones) of our high-resolution image cytometers made for the purpose of automated in vivo imaging.

  • Czech name

    Automatizované in vivo snímání buněčného obsahu s využitím fluorescenčních proteinů

  • Czech description

    Automatizované in vivo snímání buněčného obsahu s využitím fluorescenčních proteinů.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GP204%2F03%2FD031" target="_blank" >GP204/03/D031: Apoptosis-inducing factor (AIF): its translocation from mitochondria and its action on nuclear chromatin</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2004

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Cytometry

  • ISSN

    0196-4763

  • e-ISSN

  • Volume of the periodical

    59A/2004

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    1

  • Pages from-to

    107-107

  • UT code for WoS article

  • EID of the result in the Scopus database