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外来入侵植物紫茎泽兰不同组织RNA提取方法
引用本文:黄文坤,程红梅,郭建英,高必达,万方浩.外来入侵植物紫茎泽兰不同组织RNA提取方法[J].生物技术通报,2007,0(2):147-150.
作者姓名:黄文坤  程红梅  郭建英  高必达  万方浩
作者单位:1. 湖南农业大学生物安全科学技术学院,长沙,410128;植物病虫害生物学国家重点实验室,中国农业科学院植物保护研究所,北京 100094
2. 中国农业科学院生物技术研究所,北京,100081
3. 植物病虫害生物学国家重点实验室,中国农业科学院植物保护研究所,北京 100094
4. 湖南农业大学生物安全科学技术学院,长沙,410128
摘    要:从植物组织中提取高质量的RNA是进行cDNA文库构建等分子生物学研究的前提。在苯酚法的基础上,改进并得到了一种适合紫茎泽兰根、茎、叶总RNA快速提取的方法,消除了蛋白质、DNA、多糖等的污染。该方法提取的紫茎泽兰不同组织总RNA纯度高、完整性好,可用于RT-PCR、cDNA文库构建、Northern杂交等分子生物学实验,而且简单、经济、重复性好,适合于多种植物组织总RNA的提取。Northern杂交表明F3’H基因在紫茎泽兰的根、茎、叶等组织中广泛存在,但在叶中的表达量最高,在根中的表达量最低。

关 键 词:紫茎泽兰  入侵植物  RNA提取
修稿时间:2007-01-26

Method of RNA Extraction from Different Tissues of Invasive Alien Weed Eupatorium adenophorum
Huang Wenkun,Cheng Hongmei,Guo Jianying,Gao Bida,Wan Fanghao.Method of RNA Extraction from Different Tissues of Invasive Alien Weed Eupatorium adenophorum[J].Biotechnology Bulletin,2007,0(2):147-150.
Authors:Huang Wenkun  Cheng Hongmei  Guo Jianying  Gao Bida  Wan Fanghao
Institution:1.College of Bio-Safety Science and Teehnology ,Hunan Agricultural University , Changsha 410128 ; 2.Key Laboratory for Biology of Plant Diseases and Insect Pests,lnstitute of Plant Protection,Chinese Academy of Agricultural Seienees,Beijing 100094;3.Institute of b ioteehnology Research,Chinese Academy of Agricultural Seienees , Beijing 100081
Abstract:Extracting high quality RNA from plant tissues is the groundwork in carrying out researches in molecular biology such as cDNA library construction.In this study,an improved method based on the PHENOL extraction method were established to extract total RNA from roots,stems and leaves of E.adenophorum efficiently.It approved to be able to avoid protein,DNA and polysaccharide contaminations.And the total RNA extracted from different E.adenophorum tissues was of high purity and integrity,and was suitable for RT-PCR,northern blot and cDNA library construction.This method is simple,economic,quick and has good repeatability,and is also suitable for extracting total RNA from other plant species.Northern blot analysis showed that the F3'H gene expressed in the leaves,stems and roots of E.adenophorum,and the highest expression level of F3'H was detected in the leaf,then the medium in the stem,and the lowest in the root.
Keywords:RT-PCR
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