Source:http://linkedlifedata.com/resource/pubmed/id/16739216
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2006-9-21
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pubmed:abstractText |
Applications of fluorescence-activated cell sorting (FACS) are ideally performed under aseptic conditions so that isolated cells can be successfully cultured, transplanted, or processed for the isolation of protein and nucleic acids. However, modern "off-the shelf" flow cytometers are suboptimally designed for these purposes because nonsterile instrument hardware components directly contact sample-harboring fluids, compromising their sterility.
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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 |
Sep
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pubmed:issn |
1552-4949
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2006 International Society for Analytical Cytology.
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
70
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
344-54
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pubmed:dateRevised |
2009-12-11
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pubmed:meshHeading | |
pubmed:year |
2006
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pubmed:articleTitle |
Sterile and disposable fluidic subsystem suitable for clinical high speed fluorescence-activated cell sorting.
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pubmed:affiliation |
Stowers Institute for Medical Research, Kansas City, Missouri 64110, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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