Fluorescence-detected linear dichroism imaging in a re-scan confocal microscope equipped with differential polarization attachment
Author:
Funder
GINOP
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Biophysics
Link
http://link.springer.com/content/pdf/10.1007/s00249-019-01365-4.pdf
Reference36 articles.
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2. De Luca GMR, Breedijk RMP, Brandt RAJ, Zeelenberg CHC, de Jong BE, Timmermans W, Azar LN, Hoebe RA, Stallinga S, Manders EMM (2013) Re-scan confocal microscopy: scanning twice for better resolution. Biomed Opt Express 4:2644–2656. https://doi.org/10.1364/BOE.4.002644
3. De Luca GMR, Breedijk RMP, Hoebe RA, Stallinga S, Manders EMM (2017) Re-scan confocal microscopy (R. C. M.) improves the resolution of confocal microscopy and increases the sensitivity. Methods Appl Fluoresc 5:015002. https://doi.org/10.1088/2050-6120/5/1/015002
4. Djikanović D, Devečerski A, Simonović J, Matović B, Garab G, Steinbach G, Kalauzi A, Radotić K (2016) Comparison of macromolecular interactions in the cell walls of hardwood, softwood and maize by fluorescence and FTIR spectroscopy, differential polarization laser scanning microscopy and X ray diffraction. Wood Sci Technol 50:547–566. https://doi.org/10.1007/s00226-015-0792-y
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