Source:http://linkedlifedata.com/resource/pubmed/id/20006960
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2009-12-16
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pubmed:abstractText |
We report applications of two-photon excitation fluorescence (2PEF) microscopy with subdiffraction-limit resolution for green-fluorescent-protein-tagged cell imaging. The microscope integrates 2PEF microscopy and stimulated emission depletion microscopy in one microscope that has the benefits of both techniques: intrinsic three-dimensional resolution, confined photobleaching, and subdiffraction-limit resolution. The subdiffraction-limit resolution was demonstrated by resolving green-fluorescent-protein-tagged caveolar vesicles located within a distance shorter than the diffraction limit of a regular 2PEF microscope, which is approximately 250 nm even with the best optics. The full width at half-maximum of the effective point-spread function for the 2PEF microscope was estimated to be approximately 54 nm.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1542-0086
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
16
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pubmed:volume |
97
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3224-8
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pubmed:dateRevised |
2010-12-17
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pubmed:meshHeading |
pubmed-meshheading:20006960-Animals,
pubmed-meshheading:20006960-CHO Cells,
pubmed-meshheading:20006960-Cricetinae,
pubmed-meshheading:20006960-Cricetulus,
pubmed-meshheading:20006960-Green Fluorescent Proteins,
pubmed-meshheading:20006960-Microscopy, Fluorescence,
pubmed-meshheading:20006960-Molecular Imaging,
pubmed-meshheading:20006960-Photons
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pubmed:year |
2009
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pubmed:articleTitle |
Subdiffraction-limit two-photon fluorescence microscopy for GFP-tagged cell imaging.
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pubmed:affiliation |
Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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