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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
1991-8-7
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pubmed:abstractText |
Amino acids and peptides, from both standard solutions and biological samples, were successfully reacted with 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde, at low concentration, to form highly fluorescent isoindole derivatives. The formed mixtures are effectively separated by high-performance capillary electrophoresis and their constituents detected by their laser-induced fluorescence signals. The minimum detectable quantities in the low attomole (10(-18) mol) range are encountered.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0003-2700
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
63
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
408-12
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2064006-Amines,
pubmed-meshheading:2064006-Amino Acids,
pubmed-meshheading:2064006-Benzoates,
pubmed-meshheading:2064006-Electrophoresis,
pubmed-meshheading:2064006-Hydrogen-Ion Concentration,
pubmed-meshheading:2064006-Indicators and Reagents,
pubmed-meshheading:2064006-Lasers,
pubmed-meshheading:2064006-Peptides,
pubmed-meshheading:2064006-Quinolines,
pubmed-meshheading:2064006-Spectrometry, Fluorescence
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pubmed:year |
1991
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pubmed:articleTitle |
Design of 3-(4-carboxybenzoyl)-2-quinolinecarboxaldehyde as a reagent for ultrasensitive determination of primary amines by capillary electrophoresis using laser fluorescence detection.
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pubmed:affiliation |
Department of Chemistry, Indiana University, Bloomington 47405.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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