https://imaging-techniken.biologie.uni-greifswald.de/index.php?action=history&feed=atom&title=Zeiss_LEO_906Zeiss LEO 906 - Versionsgeschichte2026-04-22T02:46:20ZVersionsgeschichte dieser Seite in Imaging TechnikenMediaWiki 1.42.3https://imaging-techniken.biologie.uni-greifswald.de/index.php?title=Zeiss_LEO_906&diff=131&oldid=prevAdmin: Die Seite wurde neu angelegt: „= Type of device = Transmission electron microscope by Zeiss = Short description = A view into the interior of objects can be realized using a transmission electron microscope which produces a two-dimensional image of the specimen. For this purpose, thin slices of the specimens are generally necessary to allow the electrons to penetrate. = Instrument parameters = With this device objects can be visualized up to a 60,000-fold magnification using an ac…“2026-02-04T14:43:11Z<p>Die Seite wurde neu angelegt: „= Type of device = Transmission electron microscope by Zeiss = Short description = A view into the interior of objects can be realized using a transmission electron microscope which produces a two-dimensional image of the specimen. For this purpose, thin slices of the specimens are generally necessary to allow the electrons to penetrate. = Instrument parameters = With this device objects can be visualized up to a 60,000-fold magnification using an ac…“</p>
<p><b>Neue Seite</b></p><div>= Type of device =<br />
Transmission electron microscope by Zeiss<br />
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= Short description =<br />
A view into the interior of objects can be realized using a transmission electron microscope which produces a two-dimensional image of the specimen. For this purpose, thin slices of the specimens are generally necessary to allow the electrons to penetrate.<br />
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= Instrument parameters =<br />
With this device objects can be visualized up to a 60,000-fold magnification using an accelerating voltage of 80 kV. <br />
The microscope is equipped with a wide-angle dual speed CCD camera Sharpeye (Tröndle, Moorenweis, Germany), operated by the ImageSP software.<br />
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= Methods & Expertise =<br />
Application for life sciences research<br />
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= No expertise regarding =<br />
Material science<br />
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= Reference publications =<br />
*Lange, T., Maron, L., Weber, C., Biedenweg, D., Schlüter, R. & Endlich, N. (2025). Efficient delivery of small RNAs to podocytes ''in vitro'' by direct exosome transfection. J. Nanobiotechnol. 23(1):373<br />
*Beirow, K., Schmidt, C., Jürgen, B., Schlüter, R., Schweder, T. & Bednarski, P. J. (2024). Investigation of TGF-α-overexpressing mouse hepatocytes (TAMH) cultured as spheroids for use in hepatotoxicity screening of drug candidates. J. Appl. Toxicol. 44(2): 272-286<br />
*Hinzke, T., Kleiner, M., Meister, M., Schlüter, R., Hentschker, C., Pane-Farre, J., Hildebrandt, P., Felbeck, H., Sievert, S. M., Bonn, F., Völker, U., Becher, D., Schweder, T. & Markert, S. (2021). Bacterial symbiont subpopulations have different roles in a deep-sea symbiosis. Elife 10. Article Number: e58371<br />
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= Affiliation, Contact & Terms of use =<br />
{| border="2"<br />
|style="width:200px; text-align:left;" |Affiliation: ||style="width:500px; text-align:left;" |<br />
:University of Greifswald, Imaging Center of the Department of Biology<br />
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|Location: || <br />
:University of Greifswald<br />
:Imaging Center of the Department of Biology<br />
:Laboratory for Electron Microscopy<br />
:Friedrich-Ludwig-Jahn-Str. 16<br />
:17498 Greifswald<br />
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|Contact person: || <br />
:Dr. Rabea Schlüter<br />
:rabea.schlueter@uni-greifswald.de | Phone: 03834 420 5992<br />
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|Terms of use: || <br />
:https://imaging.uni-greifswald.de/en/general-terms-of-use/nutzungsordnungen/lem/<br />
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|Biosafety level: || <br />
:None<br />
|}</div>Admin