Source:http://linkedlifedata.com/resource/pubmed/id/19899076
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-1-27
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pubmed:abstractText |
We have developed an optimized procedure using dual size exclusion/affinity hydrogel nanoparticles to capture and comparatively analyze low molecular mass proteins directly from biological samples. The method described facilitates charge- and size-dependent protein binding, direct analysis by MS or other means and is highly reproducible. A comparative analysis of the low molecular mass proteome of plasma following freeze-thaw immediately after venipuncture is used to illustrate proof-of-concept. The technique described is rapid and may be easily reproduced in any laboratory.
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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 |
Jan
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pubmed:issn |
1615-9861
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
332-6
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
An optimized procedure for the capture, fractionation and proteomic analysis of proteins using hydrogel nanoparticles.
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pubmed:affiliation |
Prince Henrys Institute of Medical Research, Clayton, VIC 3168, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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