Integration of confocal and atomic force microscopy images (Articolo in rivista)

Type
Label
  • Integration of confocal and atomic force microscopy images (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.jneumeth.2008.09.034 (literal)
Alternative label
  • Shripad Kondraa; Jummi Laishram; Jelena Ban; Elisa Migliorini; Valentina Di Foggia; Marco Lazzarino; Vincent Torre; Maria Elisabetta Ruaro (2009)
    Integration of confocal and atomic force microscopy images
    in Journal of neuroscience methods
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Shripad Kondraa; Jummi Laishram; Jelena Ban; Elisa Migliorini; Valentina Di Foggia; Marco Lazzarino; Vincent Torre; Maria Elisabetta Ruaro (literal)
Pagina inizio
  • 94 (literal)
Pagina fine
  • 107 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 177 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • International School for Advanced Studies, Area Science Park, Basovizza 34012 Trieste, Italy Glance Vision Technologies, Area Science Park, Basovizza 34012 Trieste, Italy CBM, Area Science Park, Basovizza 34012 Trieste, Italy CNR-INFM Laboratorio TASC, Area Science Park, Basovizza 34012 Trieste, Italy (literal)
Titolo
  • Integration of confocal and atomic force microscopy images (literal)
Abstract
  • Atomic force microscopy (AFM) provides the possibility to map the 3D structure of viewed objects with a nanometric resolution, which cannot be achieved with other imaging methods such as conventional video imaging and confocal fluorescent microscopy. Video imaging with CCD cameras can provide an analysis of biological events with a temporal and spatial resolution not possible with AFM, while confocal imaging allows the simultaneous acquisition of immunofluorescence images. In this communication we present a simple method to combine AFM and confocal images to study differentiating embryonic stem (ES) cells-derived and dorsal root ganglia (DRG) neurons in culture. Neurons were grown on coverslips with micrometric markers that allow finding and imaging the same neuron with different microscopes. AFM and confocal images were registered using conventional methods used in Computer Science. The combination of these two techniques allows relating functional properties to morphological features of imaged neurons (literal)
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