Show simple item record

dc.contributor.authorAllen, Terence D
dc.contributor.authorRutherford, Sandra A
dc.contributor.authorMurray, Stephen M
dc.contributor.authorGardiner, Fiona
dc.contributor.authorKiseleva, Elena
dc.contributor.authorGoldberg, Martin W
dc.contributor.authorDrummond, Sheona P
dc.date.accessioned2009-06-23T11:28:03Z
dc.date.available2009-06-23T11:28:03Z
dc.date.issued2007
dc.identifier.citationVisualization of the nucleus and nuclear envelope in situ by SEM in tissue culture cells. 2007, 2 (5):1180-4 Nat Protocen
dc.identifier.issn1750-2799
dc.identifier.pmid17546013
dc.identifier.doi10.1038/nprot.2007.139
dc.identifier.urihttp://hdl.handle.net/10541/71224
dc.description.abstractOur previous work characterizing the biogenesis and structural integrity of the nuclear envelope and nuclear pore complexes (NPCs) has been based on amphibian material but has recently progressed into the analysis of tissue-culture cells. This protocol describes methods for the high resolution visualization, by field-emission scanning electron microscopy (FESEM), of the nucleus and associated structures in tissue culture cells. Imaging by fluorescence light microscopy shows general nuclear and NPC information at a resolution of approximately 200 nm, in contrast to the 3-5 nm resolution provided by FESEM or transmission electron microscopy (TEM), which generates detail at the macromolecular level. The protocols described here are applicable to all tissue culture cell lines tested to date (HeLa, A6, DLD, XTC and NIH 3T3). The processed cells can be stored long term under vacuum. The protocol can be completed in 5 d, including 3 d for cell growth, 1 d for processing and 1 d for imaging.
dc.language.isoenen
dc.subject.meshAnimals
dc.subject.meshCell Culture Techniques
dc.subject.meshCell Line
dc.subject.meshCell Nucleus
dc.subject.meshMicroscopy, Electron, Scanning
dc.subject.meshNuclear Envelope
dc.subject.meshXenopus laevis
dc.titleVisualization of the nucleus and nuclear envelope in situ by SEM in tissue culture cells.en
dc.typeArticleen
dc.contributor.departmentPaterson Institute for Cancer Research, University of Manchester, Wilmslow Road, Withington, Manchester M20 4BX, UK. tallen@picr.man.ac.uken
dc.identifier.journalNature Protocolsen
refterms.dateFOA2020-04-22T12:25:39Z
html.description.abstractOur previous work characterizing the biogenesis and structural integrity of the nuclear envelope and nuclear pore complexes (NPCs) has been based on amphibian material but has recently progressed into the analysis of tissue-culture cells. This protocol describes methods for the high resolution visualization, by field-emission scanning electron microscopy (FESEM), of the nucleus and associated structures in tissue culture cells. Imaging by fluorescence light microscopy shows general nuclear and NPC information at a resolution of approximately 200 nm, in contrast to the 3-5 nm resolution provided by FESEM or transmission electron microscopy (TEM), which generates detail at the macromolecular level. The protocols described here are applicable to all tissue culture cell lines tested to date (HeLa, A6, DLD, XTC and NIH 3T3). The processed cells can be stored long term under vacuum. The protocol can be completed in 5 d, including 3 d for cell growth, 1 d for processing and 1 d for imaging.


Files in this item

Thumbnail
Name:
74700.pdf
Size:
2.085Mb
Format:
PDF
Description:
From UNPAYWALL

This item appears in the following Collection(s)

Show simple item record