Volume 1 Issue 3
Aug.  2011
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Zhi-Juan Cao, Qian-Wen Peng, Xue Qiu, Cai-Yun Liu, Jian-Zhong Lu. Highly sensitive chemiluminescence technology for protein detection using aptamer-based rolling circle amplification platform[J]. Journal of Pharmaceutical Analysis, 2011, 01(3): 159-165. doi: 10.1016/j.jpha.2011.06.002
Citation: Zhi-Juan Cao, Qian-Wen Peng, Xue Qiu, Cai-Yun Liu, Jian-Zhong Lu. Highly sensitive chemiluminescence technology for protein detection using aptamer-based rolling circle amplification platform[J]. Journal of Pharmaceutical Analysis, 2011, 01(3): 159-165. doi: 10.1016/j.jpha.2011.06.002

Highly sensitive chemiluminescence technology for protein detection using aptamer-based rolling circle amplification platform

doi: 10.1016/j.jpha.2011.06.002
Funds:

the National Drug Innovative Program

the Research Fund for the Doctoral Program of Higher Education

  • Publish Date: Aug. 10, 2011
  • A robust,selective and highly sensitive chemiluminescent (CL) platform for protein assay was presented in this paper.This novel CL approach utilized rolling circle amplification (RCA) as a signal enhancement technique and the 96-well plate as the immobilization and separation carrier.Typically,the antibody immobilized on the surface of 96-well plate was sandwiched with the protein target and the aptamer-primer sequence.This aptamer-primer sequence was then employed as the primer of RCA.Based on this design,a number of the biotinylated probes and streptavidin-horseradish peroxidase (SA-HRP) were captured on the plate,and the CL signal was amplified.In summary,our results demonstrated a robust biosensor with a detection limit of 10 fM that is easy to be established and utilized,and devoid of light source.Therefore,this new technique will broaden the perspective for future development of DNA-based biosensors for the detection of other protein biomarkers related to clinical diseases,by taking advantages of high sensitivity and selectivity.
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