Volume 22, Issue 7 pp. 708-713
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Different biotinylation strategies for competitive immunoassay of estradiol

Jin-Fu Zhao

Jin-Fu Zhao

Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

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Yong-Cheng Wang

Yong-Cheng Wang

Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

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Yuan-Zong Li

Yuan-Zong Li

Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

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Wen-Bao Chang

Wen-Bao Chang

Key Laboratory of Bioorganic Chemistry and Molecular Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China

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First published: 26 August 2010
Citations: 7

Abstract

Study on biotinylation strategies for competitive immunoassay of estradiol (Ez) was carried out. Two types of competitive enzyme immunoassay (WIA) with Biotin-Avidin amplification system were established and optimized. The E2-Biotin conjugate was used as a mere in one assay, and biotinylated antibody was used as a tracer in the other. In both of EIAs, horseradish peroxidase-labelled Avidin (Avidin-HRP) was used with a spectrometric determination of enzyme activity. The precision, sensitivity and specificity were measured and compared. The results showed that although both were satisfactory in specificity, the EL4 with hapten-Biotin showed to be superior to the EL4 with biotinylated antibody in sensitivity and precision. The limit of detection of serum E2 was 8 and 50 pg/mL with E2-Biotin and biotinylated antibody as tracer, respectively.

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