File:3D-SIM-1 NPC Confocal vs 3D-SIM.jpg

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English: Comparison of resolution obtained by confocal laser scanning microscopy (clsm, left) and 3D structured illumination microscopy (3D-SIM-Microscopy, right). Top images each show a nucleus of a mouse cell, the white boxes are magnified at the bottom. Nuclear pores (anti-NPC, red) nuclear envelope (anti-Lamin, green). Chromatin/DNA (DAPI, blue). scale bars: top 5 µm, bottom 1µm. For further information see: Schermelleh L, Carlton PM, Haase S, Shao L, Winoto L, Kner P, Burke B, Cardoso MC, Agard DA, Gustafsson MG, Leonhardt H, Sedat JW (June 2008). "Subdiffraction multicolor imaging of the nuclear periphery with 3D structured illumination microscopy". Science (journal) 320 (5881): 1332–6. DOI:10.1126/science.1156947. PMID 18535242.
Deutsch: Vergleich des Auflösungsvermögen von konfokaler Laser-Scanning Mikroskopie (CLSM, links) und 3D-SIM (rechts). Zellkernporen (anti-NPC, rot), Zellkernhülle (anti-Lamin B, grün), sowie DNA verpackt in Chromatin (DAPI, blau) wurden in einer Mauszelle simultan angefärbt. Der Maßstab entspricht 5 µm (oben) und 1 µm (unten). Für weitere Informationen siehe oben zitierte Veröffentlichung.)
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Source Lothar Schermelleh
Author Lothar Schermelleh
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current17:21, 16 January 2009Thumbnail for version as of 17:21, 16 January 20091,069 × 848 (307 KB)Dietzel65 (talk | contribs){{Information |Description={{en|1=(to be added soon)}} {{de|1=Vergleich für das Auflösungsvermögen von konfokaler Laser-Scanning Mikroskopie (CLSM, links) und 3D-SIM (rechts). Zellkernporen (NPC, rot), Zellkernhülle (Lamin B, grün), sowie DNA

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