地中海贫血基因检测新技术

Lingwen Zeng, Luxin Yu, Yinghui Zhang
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引用次数: 1

摘要

等温核酸扩增是在37℃、42℃等恒温条件下快速高效积累核酸序列的简单过程。与温度循环法(如PCR)相比,等温核酸扩增方法具有几个优点,包括快速检测结果、成本效益和便携性。本章介绍了两种基于环形链位移聚合反应(CSDPR)的检测方法,以实现对地中海贫血基因的敏感和特异性检测。一种是基于CSDPR的用于地中海贫血DNA半定量检测的横向流动条带生物传感器。另一种是基于CSDPR的分光光度DNA检测方法,用于地中海贫血DNA的定量检测。
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Emerging Techniques for Thalassemia Gene Detection
Isothermal nucleic acid amplification is a simple process that rapidly and efficiently accumulates nucleic acid sequences at constant temperature such as 37 and 42°C. Isothermal nucleic acid amplification approach offers several advantages over temperature circle methods (such as PCR) including rapid assay results, cost-effectiveness, and portability. Two detection approaches based on circular strand-displacement polymerization reaction (CSDPR) were presented in this chapter for sensitive and specific thalassemia gene detection. One is a lateral flow strip biosensor based on CSDPR for semi-quantitative detection of thalassemia DNA. The other is a spectrophotometric DNA detection approach based on CSDPR for quantitative detection of thalassemia DNA.
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