rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
Pt 6
|
pubmed:dateCreated |
2003-12-3
|
pubmed:abstractText |
Dual-wavelength single-particle fluorescence imaging has been used to quantify the co-localization of receptors and/or ligands on cells by widefield microscopy. Methods for correction of chromatic aberration and identification of submicroscopic artefacts are presented, with data for the lipopolysaccharide/CD14 and MHC class II/CD74 systems.
|
pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0300-5127
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
31
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1453-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:14641088-Animals,
pubmed-meshheading:14641088-Antigens, CD14,
pubmed-meshheading:14641088-Antigens, Differentiation, B-Lymphocyte,
pubmed-meshheading:14641088-CHO Cells,
pubmed-meshheading:14641088-Cricetinae,
pubmed-meshheading:14641088-Histocompatibility Antigens Class II,
pubmed-meshheading:14641088-Microscopy, Fluorescence,
pubmed-meshheading:14641088-Receptors, Cell Surface
|
pubmed:year |
2003
|
pubmed:articleTitle |
Co-localization of cell surface receptors at high spatial resolution by single-particle fluorescence imaging.
|
pubmed:affiliation |
Department of Biological Sciences, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, U.K.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|