Source:http://linkedlifedata.com/resource/pubmed/id/18228403
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2008-1-29
|
pubmed:abstractText |
Fluorescent speckle microscopy (FSM), a combination of conventional wide-field fluorescent light microscopy and digital imaging with a low-noise, charge-coupled device (CCD) camera, has been developed to allow visualization of assembly/disassembly dynamics, movement, and turnover of macromolecule assemblies in vivo and in vitro. FSM uses a low level of fluorescent subunits to avoid high background. This produces an image of speckled molecules that co-assemble with endogenous molecules and are followed to characterize dynamic events in living cells.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1934-2616
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
Chapter 4
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
Unit 4.10
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:18228403-Actins,
pubmed-meshheading:18228403-Animals,
pubmed-meshheading:18228403-Cells,
pubmed-meshheading:18228403-Clinical Laboratory Techniques,
pubmed-meshheading:18228403-Humans,
pubmed-meshheading:18228403-Image Processing, Computer-Assisted,
pubmed-meshheading:18228403-Microscopy, Fluorescence,
pubmed-meshheading:18228403-Microtubules,
pubmed-meshheading:18228403-Research,
pubmed-meshheading:18228403-Signal Processing, Computer-Assisted
|
pubmed:year |
2002
|
pubmed:articleTitle |
Fluorescent speckle microscopy (FSM) of microtubules and actin in living cells.
|
pubmed:affiliation |
The Scripps Research Institute, La Jolla, California, USA.
|
pubmed:publicationType |
Journal Article,
Review
|