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Confocal Laser Scanning Microscopy and Two Photon Excitation Microscopy as Tools to Study Testate Amoebae
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SYSNO ASEP 0354019 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Ostatní články Title Confocal Laser Scanning Microscopy and Two Photon Excitation Microscopy as Tools to Study Testate Amoebae Author(s) Burdíková, Zuzana (FGU-C) RID
Čapek, Martin (FGU-C) RID, ORCID
Ostašov, Pavel (FGU-C)
Mitchell, E.A.D. (CH)
Machač, Jiří (BU-J)
Kubínová, Lucie (FGU-C) RID, ORCIDSource Title Microscopy and Microanalysis. - : Cambridge University Press - ISSN 1431-9276
Roč. 16, Suppl.2 (2010), s. 1142-1143Number of pages 2 s. Action Microscopy and Microanalysis 2010 Event date 01.08.2010-05.08.2010 VEvent location Portland Country US - United States Event type WRD Language eng - English Country US - United States Keywords testate amoebae ; confocal microscopy ; two-photon microscopy Subject RIV BH - Optics, Masers, Lasers R&D Projects LC06063 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GA102/08/0691 GA ČR - Czech Science Foundation (CSF) GA304/09/0733 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z50110509 - FGU-C (2005-2011) AV0Z60050516 - BU-J (2005-2011) DOI 10.1017/S1431927610060897 Annotation We applied CLSM and Two-Photon Excitation (TPE) microscopy techniques to visualize testate amoebae (TA), their test, morphology and physiology. TA are usually examined using SEM and E-SEM. It is not possible to acquire images of living TA and physiology of the amoeba inside the test by SEM or E-SEM. The goal of the study was to examine the potential of CLSM and TPE for imaging of TA. We tried 17 fluorescent dyes to label different structures of TA. CLSM enabled us to acquire images of TA from depths up to 40 μm, whereas TPE was able to penetrate to 60 μm. Stereological methods were employed to estimate the volume of the biomass of TA visualized by CLSM Workplace Institute of Physiology Contact Lucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400 Year of Publishing 2011
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