caa a22 4500 445840250 CHVBK 20180317145341.0 cr unu---uuuuu 170323e20110101xx s 000 0 eng 10.1007/s00709-010-0233-6 doi (NATIONALLICENCE)springer-10.1007/s00709-010-0233-6 Imaging plasmodesmata [Elektronische Daten] [Karen Bell, Karl Oparka] At only 50nm in diameter, plasmodesmata (PD) are below the limit of resolution of conventional light microscopy. Consequently, much of our current interpretation of the substructure of PD is derived from transmission electron microscopy. However, PD can be imaged with alternative techniques, including field emission scanning electron microscopy and ‘super-resolution' imaging approaches such as 3D-structured illumination microscopy. This review considers the methods currently available for studying PD and focuses on the boundary between light- and electron-based imaging approaches. Springer-Verlag, 2010 Plasmodesmata nationallicence Transmission electron microscopy nationallicence 3D-structured illumination microscopy nationallicence Bell Karen Institute of Molecular Plant Sciences, University of Edinburgh, Mayfield Road, EH9 3JR, Edinburgh, UK aut Oparka Karl Institute of Molecular Plant Sciences, University of Edinburgh, Mayfield Road, EH9 3JR, Edinburgh, UK aut Protoplasma Springer Vienna 248/1(2011-01-01), 9-25 0033-183X 248:1<9 2011 248 709 https://doi.org/10.1007/s00709-010-0233-6 text/html Onlinezugriff via DOI 1 review-article jats NATIONALLICENCE 856 40 https://doi.org/10.1007/s00709-010-0233-6 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Bell Karen Institute of Molecular Plant Sciences, University of Edinburgh, Mayfield Road, EH9 3JR, Edinburgh, UK aut NATIONALLICENCE 700 1- Oparka Karl Institute of Molecular Plant Sciences, University of Edinburgh, Mayfield Road, EH9 3JR, Edinburgh, UK aut NATIONALLICENCE 773 0- Protoplasma Springer Vienna 248/1(2011-01-01), 9-25 0033-183X 248:1<9 2011 248 709 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer