pubmed-article:18548750 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C0231881 | lld:lifeskim |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C0185125 | lld:lifeskim |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C2349975 | lld:lifeskim |
pubmed-article:18548750 | lifeskim:mentions | umls-concept:C1627358 | lld:lifeskim |
pubmed-article:18548750 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:18548750 | pubmed:dateCreated | 2008-12-1 | lld:pubmed |
pubmed-article:18548750 | pubmed:abstractText | In this paper, a sensitive resonance light scattering (RLS) method for the determination of protein is reported. In the Tris-HCl (pH 7.50) buffer, protein enhanced the RLS intensity of the Y(3+)-2-thenoyltrifluoroacetone (TTA)-sodium dodecyl sulphate (SLS) system. The enhanced RLS intensities were in proportion to the concentrations of proteins in the range 8.0 x 10(-9)-1.0 x 10(-5) g/mL for BSA, 1.0 x 10(-8)-1.0 x 10(-5) g/mL for HSA and 1.0 x 10(-8)-1.0 x 10(-6 )g/mL for EA, and their detection limits were 5.0, 5.4 and 6.7 ng/mL, respectively. Actual samples were satisfactorily determined. The interaction mechanism was also studied. | lld:pubmed |
pubmed-article:18548750 | pubmed:language | eng | lld:pubmed |
pubmed-article:18548750 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18548750 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18548750 | pubmed:issn | 1522-7243 | lld:pubmed |
pubmed-article:18548750 | pubmed:author | pubmed-author:XuWeiW | lld:pubmed |
pubmed-article:18548750 | pubmed:author | pubmed-author:YangJingheJ | lld:pubmed |
pubmed-article:18548750 | pubmed:author | pubmed-author:WuXiaX | lld:pubmed |
pubmed-article:18548750 | pubmed:author | pubmed-author:GuoChangyingC | lld:pubmed |
pubmed-article:18548750 | pubmed:copyrightInfo | (c) 2008 John Wiley & Sons, Ltd. | lld:pubmed |
pubmed-article:18548750 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18548750 | pubmed:volume | 23 | lld:pubmed |
pubmed-article:18548750 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18548750 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18548750 | pubmed:pagination | 404-9 | lld:pubmed |
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pubmed-article:18548750 | pubmed:articleTitle | Resonance light-scattering enhancement effect of the protein-Y3+-TTA-SLS system and its analytical application. | lld:pubmed |
pubmed-article:18548750 | pubmed:affiliation | Key Laboratory of Colloid and Interface Chemistry (Shandong University), Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, Shandong, People's Republic of China. | lld:pubmed |
pubmed-article:18548750 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18548750 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |