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首页> 外文期刊>Journal of Bioactive and Compatible Polymers >Use of a chitosan-cadmium polymer as a redox hybridization indicator for CaMV35S promoter gene detection
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Use of a chitosan-cadmium polymer as a redox hybridization indicator for CaMV35S promoter gene detection

机译:壳聚糖-镉聚合物作为CaMV35S启动子基因检测的氧化还原杂交指示剂的用途

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摘要

A water-soluble chitosan-coordinated cadmium polymer was synthesized, and its recognition of single-stranded and double-stranded DNA was investigated. The electrochemical analysis in the homogeneous solutions revealed that the chitosan-coordinated cadmium polymer association with a single stranded DNA was 48 times greater than with double-stranded DNA due to the different interaction with the two kinds of DNA. The surface-based electrochemically absorbed chitosan-coordinated cadmium polymer molecules were easily removed from the double-stranded DNA-modified electrode via rinsing but could not be removed from a single-stranded DNA-modified electrode. Based on this fact, the polymer was utilized as a redox indicator for DNA hybridization detection, as the polymer was able to recognize complementary, noncomplementary, and base-mismatched sequences with a low background interference. The target DNA sequence was quantified from 5.0 x 10~(-9) to 5.0 x 10~(-7) M with a detection limit of 4.2 x 10~(-9) M. The polymerase chain reaction amplification of DNA from the real sample of a kind of transgenically modified soybeans was also detected satisfactorily.
机译:合成了水溶性壳聚糖配位的镉聚合物,研究了其对单链和双链DNA的识别。在均相溶液中的电化学分析表明,由于与两种DNA的相互作用不同,壳聚糖配位的镉聚合物与单链DNA的缔合比双链DNA的缔合大48倍。基于表面的电化学吸收的壳聚糖配位的镉聚合物分子很容易通过冲洗从双链DNA修饰的电极上除去,但不能从单链DNA修饰的电极上除去。基于这一事实,该聚合物被用作DNA杂交检测的氧化还原指示剂,因为该聚合物能够以低背景干扰识别互补,非互补和碱基错配的序列。靶DNA序列的定量范围为5.0 x 10〜(-9)M至5.0 x 10〜(-7)M,检测限为4.2 x 10〜(-9)M。还令人满意地检测到一种转基因大豆的样品。

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