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一种新型的通用引物-多重 PCR 方法与测序凝胶电泳分析。

A novel universal primer-multiplex-PCR method with sequencing gel electrophoresis analysis.

机构信息

Laboratory of Food Safety, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing, China.

出版信息

PLoS One. 2012;7(1):e22900. doi: 10.1371/journal.pone.0022900. Epub 2012 Jan 17.

Abstract

In this study, a novel universal primer-multiplex-PCR (UP-M-PCR) method adding a universal primer (UP) in the multiplex PCR reaction system was described. A universal adapter was designed in the 5'-end of each specific primer pairs which matched with the specific DNA sequences for each template and also used as the universal primer (UP). PCR products were analyzed on sequencing gel electrophoresis (SGE) which had the advantage of exhibiting extraordinary resolution. This method overcame the disadvantages rooted deeply in conventional multiplex PCR such as complex manipulation, lower sensitivity, self-inhibition and amplification disparity resulting from different primers, and it got a high specificity and had a low detection limit of 0.1 ng for single kind of crops when screening the presence of genetically modified (GM) crops in mixture samples. The novel developed multiplex PCR assay with sequencing gel electrophoresis analysis will be useful in many fields, such as verifying the GM status of a sample irrespective of the crop and GM trait and so on.

摘要

在这项研究中,描述了一种新型的通用引物多重 PCR(UP-M-PCR)方法,即在多重 PCR 反应体系中添加了一个通用引物(UP)。在每个特异性引物对的 5'-端设计了一个通用接头,该接头与每个模板的特异性 DNA 序列匹配,也可用作通用引物(UP)。PCR 产物在测序凝胶电泳(SGE)上进行分析,该方法具有出色的分辨率优势。该方法克服了传统多重 PCR 的一些固有缺点,如操作复杂、灵敏度较低、不同引物之间的自我抑制和扩增差异等,在对混合样品中转基因作物(GM)的存在进行筛选时,具有较高的特异性和较低的检测限,可达 0.1ng 单一种类的作物。该新型测序凝胶电泳分析多重 PCR 检测方法将在许多领域具有重要的应用价值,例如验证样品的 GM 状态,而无需考虑作物和 GM 特性等。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a497/3260127/03ed29584e65/pone.0022900.g001.jpg

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