荧光
DNA
荧光染料
G-四倍体
化学
复式(建筑)
检出限
双绞线
生物物理学
实时聚合酶链反应
生物化学
生物
色谱法
基因
物理
量子力学
作者
Lingli Zhang,Naxiu Mi,Youyu Zhang,Mingjie Wei,Haitao Li,Shouzhuo Yao
出处
期刊:Analytical Methods
[The Royal Society of Chemistry]
日期:2013-01-01
卷期号:5 (21): 6100-6100
被引量:16
摘要
A simple label-free Pb2+ fluorescent aptasensor was proposed in this work. It is known that SYBR Green1 can embed into double-stranded DNA resulting in fluorescence enhancement, but it cannot bind to the G-quadruplex formed by Pb2+ and PS2.M. In the absence of Pb2+, SYBR Green1 intercalated into the double-stranded DNA hybridized between PS2.M and its complementary strand and the fluorescence was greatly enhanced. In the presence of Pb2+, a compact G-quadruplex structure was formed and the double-stranded structure was destroyed, releasing SYBR Green1 and causing the fluorescence intensity to significantly decrease. The detection limit of the sensor was as low as 3 nM. This proposed assay strategy was a low-cost detection method for Pb2+ with high sensitivity and good selectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI