Fixation methods for electron microscopy of human and other liver

doi:10.3748/wjg.v16.i23.2851

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Jun 21, 2010; 16(23): 2851-2866
Published online Jun 21, 2010. doi: 10.3748/wjg.v16.i23.2851

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Figure 2 Transmission electron microscopy (TEM) image of an ultrathin section of a plastic-embedded liver sinusoidal endothelial cell after isolation. In the upper part of the picture is a small portion of the nucleus. The labyrinth-like structures in the cytoplasm represent fenestrae that are internalized during the isolation procedure. Electron-dense granules represent lysosomes that reflect the high digestive capacity of these cells. Magnification 6300 ×.

Citation: Wisse E, Braet F, Duimel H, Vreuls C, Koek G, Olde Damink SW, van den Broek MA, De Geest B, Dejong CH, Tateno C, Frederik P. Fixation methods for electron microscopy of human and other liver. World J Gastroenterol 2010; 16(23): 2851-2866
URL: https://www.wjgnet.com/1007-9327/full/v16/i23/2851.htm
DOI: https://dx.doi.org/10.3748/wjg.v16.i23.2851

Wisse E, Braet F, Duimel H, Vreuls C, Koek G, Olde Damink SW, van den Broek MA, De Geest B, Dejong CH, Tateno C, Frederik P. Fixation methods for electron microscopy of human and other liver. World J Gastroenterol 2010; 16(23): 2851-2866 [PMID: 20556830 DOI: 10.3748/wjg.v16.i23.2851]

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