摘要
MUC1 is a highly glycosylyted and large-molecular-weight glycoprotein, mainly expressed highly abnormal in breast cancer cells. Its specificity is higher than tissue polypeptide antigen, and its sensitivity is higher than cancer embryo antigen. Therefore, MUC1 possesses great clinical value in the diagnosis of breast cancer, and the development of a highly sensitive detecting method for MUC1 protein plays a more important role for clinical diagnosis. In the present study, sensitive detecting method for MUC1 was based on nucleic acid aptamer-rollong circle amplification (RCA) and graphene oxid-fluorescence resonance energy transfer (GO-FRET). The results show that, the linear range of quantitative detection can reach 50~1 000 pg/mL, and the limit of detection is 28.05 pg/mL, the limit of quantitation is 45.57 pg/mL. The recovery of MUC1 in human serum can be ranged from 96% to 104%.
| 投稿的翻译标题 | Quantitative Detection of MUC1 Protein by Aptamer-Based Fluorescence Analysis |
|---|---|
| 源语言 | 繁体中文 |
| 页(从-至) | 1-5 |
| 页数 | 5 |
| 期刊 | Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology |
| 卷 | 39 |
| DOI | |
| 出版状态 | 已出版 - 1 6月 2019 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
关键词
- Aptamer
- Fluorescence resonance energy transfer
- Graphene oxid
- MUC1
- RCA
指纹
探究 '基于核酸适配体的荧光分析法定量检测MUC1粘蛋白' 的科研主题。它们共同构成独一无二的指纹。引用此
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