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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Chitosan functionalized magnetic particle-assisted detection of genetically modified soybeans based on polymerase chain reaction and capillary electrophoresis
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Chitosan functionalized magnetic particle-assisted detection of genetically modified soybeans based on polymerase chain reaction and capillary electrophoresis

机译:基于聚合酶链反应和毛细管电泳的壳聚糖功能化磁粉辅助检测转基因大豆

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摘要

The high quality of DNA template is one of the key factors to ensure the successful execution of polymerase chain reaction (PCR). Therefore, development of DNA extraction methods is very important. In this work, chitosan modified magnetic particles (MPs) were synthesized and employed for extraction of genomic DNA from genetically modified (GM) soybeans. The extraction protocol used aqueous buffers for DNA binding to and releasing from the surface of the MPs based on the pH inducing the charge switch of amino groups in chitosan modified MPs. The extracted DNA was pure enough (A (&_(260)/A _(280) = 1.85) to be directly used as templates for PCR amplification. In addition, the PCR products were separated by capillary electrophoresis for screening of GM organisms. The developed DNA extraction method using chitosan modified MPs was capable of preparation of DNA templates, which were PCR inhibitor free and ready for downstream analysis. The whole process for DNA extraction and detection was preferable to conventional methods (phenol-chloroform extraction, PCR, and gel electrophoresis) due to its simplicity and rapidity as well as its avoiding the use of toxic reagents and PCR inhibitors.
机译:DNA模板的高质量是确保成功执行聚合酶链反应(PCR)的关键因素之一。因此,开发DNA提取方法非常重要。在这项工作中,合成了壳聚糖修饰的磁性颗粒(MPs),并用于从转基因(GM)大豆中提取基因组DNA。提取方案使用水性缓冲液,基于pH值诱导壳聚糖修饰的MPs中氨基的电荷转换,从而使DNA与MPs结合并从MPs表面释放。提取的DNA纯度足够高(A(&(260)/ A _(280)= 1.85),可以直接用作PCR扩增的模板,此外,PCR产物通过毛细管电泳分离以筛选GM生物。利用壳聚糖修饰的MPs开发的DNA提取方法能够制备无PCR抑制剂且可用于下游分析的DNA模板,整个DNA提取和检测过程优于常规方法(苯酚-氯仿提取,PCR和凝胶电泳)电泳技术),因为它简单,快速并且避免使用有毒试剂和PCR抑制剂。

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