Title of article :
Comparison between conventional indirect competitive enzyme-linked immunosorbent assay (icELISA) and simplified icELISA for small molecules Original Research Article
Author/Authors :
Jing Zhao، نويسنده , , Gang Li، نويسنده , , Guo-Xiang Yi، نويسنده , , Baomin Wang، نويسنده , , Aixing Deng، نويسنده , , Tiegui Nan، نويسنده , , Zhaohu Li، نويسنده , , Qing X. Li، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
7
From page :
79
To page :
85
Abstract :
A simplified indirect competitive enzyme-linked immunosorbent assay (icELISA) for small molecules was established by modifying the procedure of conventional icELISA. The key change was that the analyte, antibody, and enzyme-labeled second antibody in the simplified icELISA were added in one step, whereas in conventional icELISA these reagents were added in two separate steps. Three small chemicals, namely zeatin riboside, glycyrrhetinic acid, and chlorimuron-ethyl, were used to verify the new assay format and compare the results obtained from conventional icELISA and simplified icELISA. The results indicated that, under optimized conditions, the new assay offered several advantages over the conventional icELISA, which are simpler, less time consuming and higher sensitive although it requires more amount of reagents. The assay sensitivity (IC50) was improved for 1.2–1.4-fold. Four licorice roots samples were analyzed by conventional icELISA and simplified icELISA, as well as liquid chromatography (LC). There was no significant difference among the content obtained from the three methods for each sample. The correlation between data obtained from conventional icELISA and simplified icELISA analyses was 0.9888. The results suggest that the simplified icELISA be useful for high throughput screening of small molecules.
Keywords :
icELISA , Zeatin riboside , Chlorimuron-ethyl , Glycyrrhetinic acid , Small molecules
Journal title :
Analytica Chimica Acta
Serial Year :
2006
Journal title :
Analytica Chimica Acta
Record number :
1035954
Link To Document :
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