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  • Fluorescence microscopy has become the leading technology to study structure and dynamics of cellular components and processes. Fluorescent proteins allow us to study protein dynamics, localization, and interactions in living cells. In our laboratory, we have been developing special systems for automated cell image acquisition and analysis using fluorescence microscopy working up to five dimensions (x, y, z, t, lambda), whose hardware and software was optimized for studies on living cells. The presentation will focus on the latest developments in our technology. Besides microscopy hardware and software, also examples of possible applications will be presented. For the first time, we discovered interaction of apoptotic proteins AIF and endonuclease G, expressed using one DNA plasmid, in living human cells during apoptotic cell death.
  • Fluorescence microscopy has become the leading technology to study structure and dynamics of cellular components and processes. Fluorescent proteins allow us to study protein dynamics, localization, and interactions in living cells. In our laboratory, we have been developing special systems for automated cell image acquisition and analysis using fluorescence microscopy working up to five dimensions (x, y, z, t, lambda), whose hardware and software was optimized for studies on living cells. The presentation will focus on the latest developments in our technology. Besides microscopy hardware and software, also examples of possible applications will be presented. For the first time, we discovered interaction of apoptotic proteins AIF and endonuclease G, expressed using one DNA plasmid, in living human cells during apoptotic cell death. (en)
Title
  • Automated spinning disk confocal microscopy in 3D live cell imaging
  • Automated spinning disk confocal microscopy in 3D live cell imaging (en)
skos:prefLabel
  • Automated spinning disk confocal microscopy in 3D live cell imaging
  • Automated spinning disk confocal microscopy in 3D live cell imaging (en)
skos:notation
  • RIV/00216224:14330/10:00043375!RIV11-MSM-14330___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(2B06052), P(LC535), S, Z(MSM0021622419)
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 304459
http://linked.open...ai/riv/idVysledku
  • RIV/00216224:14330/10:00043375
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • confocal microscopy; living cells; fluorescence (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...ontrolniKodProRIV
  • [833C3E253BC5]
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...iv/tvurceVysledku
  • Matula, Pavel
  • Kozubek, Michal
  • Vařecha, Miroslav
http://linked.open...n/vavai/riv/zamer
http://localhost/t...ganizacniJednotka
  • 14330
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