| pubmed-article:16206150 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0680730 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0009742 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0596837 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0231881 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0449851 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C1148554 | lld:lifeskim |
| pubmed-article:16206150 | lifeskim:mentions | umls-concept:C0146951 | lld:lifeskim |
| pubmed-article:16206150 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:16206150 | pubmed:dateCreated | 2006-1-31 | lld:pubmed |
| pubmed-article:16206150 | pubmed:abstractText | Resonance light scattering (RLS) of Congo red (CR) was greatly enhanced by BSA (HSA) in the presence of Triton X-100 (TX-100). In sodium citrate-HCl buffer (pH 2.7-3.0), the enhanced intensity of resonance light scattering at 360 nm was in proportion to the concentration of proteins [corrected] The linear relationship was obtained between the resonance light scattering intensity and proteins in the range 5.0 x 10(-8)-8.0 x 10(-6) g/mL and 1.0 x 10(-9)-6.0 x 10(-6) g/mL for BSA and HSA, respectively. Their detection limits were 1.4 x 10(-8) g/mL and 2.8 x 10(-10) g/mL (S:N = 3), respectively. Synthetic and actual samples were analysed satisfactorily. | lld:pubmed |
| pubmed-article:16206150 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16206150 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16206150 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16206150 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16206150 | pubmed:issn | 1522-7235 | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:WuTaoT | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:YangJingheJ | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:WuXiaX | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:SunChangxiaC | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:SunShunaS | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:GuoChangyingC | lld:pubmed |
| pubmed-article:16206150 | pubmed:author | pubmed-author:ZhouChengrong... | lld:pubmed |
| pubmed-article:16206150 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16206150 | pubmed:volume | 21 | lld:pubmed |
| pubmed-article:16206150 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16206150 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16206150 | pubmed:pagination | 56-61 | lld:pubmed |
| pubmed-article:16206150 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:meshHeading | pubmed-meshheading:16206150... | lld:pubmed |
| pubmed-article:16206150 | pubmed:articleTitle | Resonance light scattering technique for the determination of proteins with Congo red and Triton X-100. | lld:pubmed |
| pubmed-article:16206150 | pubmed:affiliation | Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, Shandong, People's Republic of China. | lld:pubmed |
| pubmed-article:16206150 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16206150 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
