Source:http://linkedlifedata.com/resource/pubmed/id/12899959
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0012854,
umls-concept:C0016315,
umls-concept:C0020202,
umls-concept:C0137873,
umls-concept:C0181496,
umls-concept:C0920585,
umls-concept:C1510438,
umls-concept:C1511790,
umls-concept:C1522240,
umls-concept:C1522485,
umls-concept:C1527178,
umls-concept:C1705425,
umls-concept:C1705938,
umls-concept:C1880497,
umls-concept:C1996904,
umls-concept:C2603343
|
pubmed:issue |
4-5
|
pubmed:dateCreated |
2003-8-5
|
pubmed:abstractText |
In this paper, we present different ways to detect DNA hybridization on a solid support. The grafting chemistry is based on the electro-controlled copolymerization of a pyrrole-modified oligonucleotide and pyrrole. This process allows an easy functionalization of conducting materials. Three kind of devices were studied: silicon chips bearing an array of addressable 50 or 4 microm microelectrodes, quartz crystal microbalance (QCM) and a non patterned gold/glass slide bearing 500 microm spots. Each device is compatible with a specific detection process: a classical indirect fluorescence detection for the microchips, a microgravimetric measurement for the QCM and a surface plasmon resonance imaging process (SPRi) for the gold slides. Both QCM and SPRi are a label-free real time detection process whereas the fluorescence methodology gives end-point data but only the fluorescence and the SPRi give multiparametric results. Although the hybridization experiments show that the detection limit for an oligonucleotide is better for the fluorescence (1-10 pM) than that found for SPRi (10 nM) and QCM (250 nM), the information content of real time measurement techniques such as SPRi is of interest for many biological studies.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0731-7085
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
8
|
pubmed:volume |
32
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
687-96
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:12899959-DNA,
pubmed-meshheading:12899959-Electrochemistry,
pubmed-meshheading:12899959-Fluorescence,
pubmed-meshheading:12899959-Nucleic Acid Hybridization,
pubmed-meshheading:12899959-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:12899959-Polymers,
pubmed-meshheading:12899959-Pyrroles
|
pubmed:year |
2003
|
pubmed:articleTitle |
Polypyrrole based DNA hybridization assays: study of label free detection processes versus fluorescence on microchips.
|
pubmed:affiliation |
Département de Recherche sur la Matière Condensée, UMR 5819 (CEA, CNRS, Université J. Fourier), CEA-Grenoble, 17 Rue des Martyrs, 38054 Grenoble Cedex 09, France. tlivache@cea.fr
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|