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基于多重PCR的DNA Marker制备方法
引用本文:张俊河,王俐,董卫华,王芳,王天云. 基于多重PCR的DNA Marker制备方法[J]. 生物技术通报, 2010, 0(12)
作者姓名:张俊河  王俐  董卫华  王芳  王天云
作者单位:新乡医学院生物化学与分子生物学教研室,新乡,453003
基金项目:河南省科技厅科技攻关资助项目(0624410041); 河南省教育厅自然科学基金(2008A310008)
摘    要:报道了一种简便的制备分子量大小为100-1000bp DNA marker的方法,其原理是以一段特异的DNA片段为模板,设计PCR引物,采用多重PCR的方法一次扩增100-1000bp系列条带,酚/氯仿抽提,乙醇沉淀,即可得到条带清晰的DNA marker。

关 键 词:DNA marker  PCR  凝胶电泳  制备  

A Simple Method for Prepareing DNA Marker
Zhang Junhe,Wang Li,Dong Weihua,Wang Fang,Wang Tianyun. A Simple Method for Prepareing DNA Marker[J]. Biotechnology Bulletin, 2010, 0(12)
Authors:Zhang Junhe  Wang Li  Dong Weihua  Wang Fang  Wang Tianyun
Affiliation:Zhang Junhe Wang Li Dong Weihua Wang Fang Wang Tianyun(Department of Biochemistry and Molecular Biology,Xinxiang Medical University,Xinxiang 453003)
Abstract:A simple method that prepare DNA marker is reported in this paper.A specific DNA fragment was used as PCR template,and multiple PCR was used to amplify 100-1 000 bp series DNA fragments,and then were purified and electrophoresised in 2% agarose gels,the bands of the prepared DNA marker were clear and could be used in the molecular experiments.
Keywords:DNA marker PCR Gel electrophoresis Preparation  
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