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忽地笑不同器官RNA提取方法比较研究 被引量:1

Comparative Study on RNA Extraction Methods in Different Organs of Lycoris aurea Herb
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摘要 [目的]建立忽地笑不同器官总RNA最佳提取方法。[方法]以忽地笑鳞茎、叶、花葶和花器官为材料,分别用普通试剂盒法、多糖多酚试剂盒法、Trizol法、SDS法和CTAB法进行不同器官总RNA提取方法比较。[结果]忽地笑不同器官最佳RNA提取方法不同,仅Trizol法能提取出鳞茎中RNA,普通试剂盒法和CTAB法均能提取出叶和花器官高质量RNA,多糖多酚试剂盒法和CTAB法能提取出花葶高质量RNA。[结论]普通试剂盒法是忽地笑叶和花的最快速、最简便的提取方法;多糖多酚试剂盒法是提取花葶的最佳提取方法;CTAB法能有效去除多糖、多酚,适合忽地笑叶、花葶和花中总RNA提取;试剂盒法和CTAB法均能提取高质量RNA,满足RT-PCR及后续试验的要求。 [Objective]To establish the best extraction method of total RNA from different organs of Lycoris aurea.[Methods]The methods of extraction of total RNA from bulb,leaf,calyx and flower different organs were compared by means of common reagent box method,polysaccharide polyphenol reagent box method,Trizol method,SDS method and CTAB method.[Result]The best RNA extraction method for different organs was different.Only Trizol method can extract RNA from bulbs,and both normal reagent box method and CTAB method could extract high-quality RNA from leaves and flower organs.Polysaccharide polyphenol reagent boxed method and CTAB method could extract high-quality RNA from calyx.[Conclusion]The common reagent box method is the fastest and simplest method for extraction of Lycoris aurea leaves and flowers.The polysaccharide polyphenol reagent box method is the best method for extraction of calyx.The CTAB method can effectively remove polysaccharides and polyphenols,which is suitable for the extraction of total RNA in Lycoris aurea leaves,calyx and flowers.The reagent box method and CTAB method can extract high-quality RNA to meet the requirements of RT-PCR and subsequent tests.
作者 樊青玲 周日宝 刘湘丹 陈娅 FAN Qing-ling;ZHOU Ri-bao;LIU Xiang-dan(Changde Vocational and Technical College,Changde,Hunan 415000;TCM University of Hunan,Changsha,Hunan 410000)
出处 《安徽农业科学》 CAS 2020年第18期169-172,共4页 Journal of Anhui Agricultural Sciences
基金 中央引导地方科技发展专项资金项目(2017XF5044) 湖湘中药资源保护与利用2011协同创新中心项目(湘教通〔2015〕351) 湖南中医药大学中药学一流建设学科(校行科学〔2018〕3号)。
关键词 忽地笑 不同器官 RNA提取方法 RT-PCR Lycoris aurea Herb Different organs Extraction method of RNA RT-PCR
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