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3种制备猪肺炎支原体DNA模板方法的探讨
引用本文:张旭,武昱孜,白方方,刘茂军,华利忠,邵国青.3种制备猪肺炎支原体DNA模板方法的探讨[J].中国农学通报,2013,29(29):52-56.
作者姓名:张旭  武昱孜  白方方  刘茂军  华利忠  邵国青
作者单位:1. 江苏省农业科学院兽医研究所家畜重大疫病防控研究室2. 江苏省农业科学院兽医研究所/农业部兽用生物制品工程技术重点实验室/国家兽用生物制品工程技术研究中心3. 江苏省农业科学院兽医所
摘    要:为了筛选出一种快速、高效、廉价提取猪肺炎支原体模板DNA的方法,本研究分别对试剂盒法、双蒸水煮法、酚-氯仿法进行比较,从中选出最佳提取方法。结果显示:这3种方法均适合由菌液中提取基因组DNA;水煮法不能由组织中提取出基因组DNA,试剂盒法可由组织中提取出基因组DNA且得到的目的DNA较纯,但每次提取量少;酚-氯仿法能大批量提取组织基因组DNA,但操作繁琐,易污染且稍有杂带。针对不同的模板,选择合适的DNA制备方法,有利于做出准确检测、提高检测效率,为疾病的早期诊断提供保障。

关 键 词:分析  分析  
收稿时间:2013/4/17 0:00:00
修稿时间:6/8/2013 12:00:00 AM

Study of Three Methods for Making DNA Templates of Mycoplamsa hyopneumoniae
Zhang Xu,Wu Yuzi,Bai Fangfang,Liu Maojun,Hua Lizhong,Shao Guoqing.Study of Three Methods for Making DNA Templates of Mycoplamsa hyopneumoniae[J].Chinese Agricultural Science Bulletin,2013,29(29):52-56.
Authors:Zhang Xu  Wu Yuzi  Bai Fangfang  Liu Maojun  Hua Lizhong  Shao Guoqing
Institution:(Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences/Key Laboratory of Animal Diseases Diagnostic and Immunology, Ministry of Agriculture/National Center for Engineering Research of Veterinary Bio-products, Nanjing 210014)
Abstract:In order to filter out a fast, efficient, inexpensive method to extract the Mycoplasma hyopneumoniae DNA tempiate. In this study we compared Tissue DNA Kit, double distilled boiled method and phenol-chloroform method to choose a best way to extract Mhp DNA. The results showed that the three methods were suitable for the extraction of genomic DNA of the bacterium, however, double distilled boiling method could not extracted genomic DNA from the tiusse, the Tissue DNA Kit could extract out of genomic DNA purely from the tissue, but got a small quantity of DNA each time, phenol-chloroform method could extract large DNA of the tissue, but complicated to operate, vulnerable to pollution, and with a little impurity bands. Acorrding to the different templates, select the appropriate DNA preparation method which is beneficial to make the detection accurated, meanwhile improve the detection efficiency, to provide protection for the early disease detection.
Keywords:Plolymerase chain reaction detection
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