基于pcr检测试剂盒的中药茯苓鉴别试剂盒的研制与评价

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial Dna Part a Pub Date : 2018-01-02 DOI:10.1080/24701394.2016.1248429
Xiaomei Zhang, Tingting Zhou, Wenjing Yu, Jinxia Ai, Xuesong Wang, Lijun Gao, G. Yuan, Mingcheng Li
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引用次数: 8

摘要

摘要:研制了一种棘豆DNA检测试剂盒,对其特异性、敏感性、稳定性等指标进行了评价,并与2010年版《中国药典》中所载方法进行了比较。根据Z. dhumnades细胞色素b (Cyt b)基因的特点,结合PCR技术,采用生物信息学技术设计引物、测序和blast。试剂盒核酸提取效率按照药典方法进行。反复冻融20次后,试剂盒稳定性结果证明是有效的。灵敏度结果表明,试剂盒最低检出量为0。每样025g。试剂盒特异性试验为100%特异性。所有可重复性测试在进行三次时均显示相同的结果。与《中国药典》方法相比,本研究建立的pcr检测试剂盒准确、有效、简便、快速,在黄连药材质量检测中具有广阔的应用前景。
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Development and evaluation of a PCR-based assay kit for authentication of Zaocys dhumnades in traditional Chinese medicine
Abstract We developed a kind of Zaocys dhumnades DNA test kit and it’s indexes including specificity, sensitivity and stability were evaluated and compared with the method recorded in Chinese Pharmacopoeia (2010 edition). The bioinformatics technology was used to design primers, sequencing and blast, in conjunction with PCR technology based on the characteristics of Z. dhumnades cytochrome b (Cyt b) gene. The efficiency of nucleic acid extraction by the kit was done in accordance with Pharmacopoeia method. The kit stability results proved effective after repeated freezing and thawing 20 times. The sensitivity results indicated that the lowest amount detected by the kit was 0. 025 g of each specimen. The specificity test of the kit was 100% specific. All repeatability tests indicated the same results when conducted three times. Compared with the method recorded in Chinese Pharmacopoeia, the PCR-based assay kit by our team developed is accurate, effective in identification of Z. dhumnades, it is simple and fast, demonstrating a broad prospect in quality inspection of Z. dhumnades in the future.
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来源期刊
Mitochondrial Dna Part a
Mitochondrial Dna Part a Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.00
自引率
0.00%
发文量
6
期刊介绍: Mitochondrial DNA Part A publishes original high-quality manuscripts on physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism, and/or interactions. Manuscripts on cytosolic and extracellular mtDNA, and on dysfunction caused by alterations in mtDNA integrity as well as methodological papers detailing novel approaches for mtDNA manipulation in vitro and in vivo are welcome. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The Journal also considers manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences, as well as papers that discuss the utility of mitochondrial DNA information in medical studies and in human evolutionary biology.
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