{"title":"A Rapid Method for Analysis of cDNA Synthesis Using Ion-Pair Reversed-Phase High Performance Liquid Chromatography","authors":"M. Matin, D. Hornby","doi":"10.22067/JCMR.V11I2.83212","DOIUrl":null,"url":null,"abstract":"We have developed a rapid, quantitative method for analysing the outcome of the first strand synthesis step in cDNA library preparation, yield and molecular weight range of the final cDNA products are determined after size fractionation. This method involves conventional cDNA library construction including all enzymatic steps usually required, but replaces radioactive labelling of nucleic acids with fluorescence detection. The separation and quantification steps all involve ion-pair reversed-phase high performance liquid chromatography (IP RP HPLC). This quantitative method replaces the use of autoradiography and size exclusion chromatography with combined ion-pair reversed-phase high performance liquid chromatography and in line fluorescence detection. The result of this approach is combination of speed with the generation of reproducible, high quality cDNA libraries.","PeriodicalId":30607,"journal":{"name":"Journal of Cell and Molecular Research","volume":"11 1","pages":"55-58"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cell and Molecular Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22067/JCMR.V11I2.83212","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We have developed a rapid, quantitative method for analysing the outcome of the first strand synthesis step in cDNA library preparation, yield and molecular weight range of the final cDNA products are determined after size fractionation. This method involves conventional cDNA library construction including all enzymatic steps usually required, but replaces radioactive labelling of nucleic acids with fluorescence detection. The separation and quantification steps all involve ion-pair reversed-phase high performance liquid chromatography (IP RP HPLC). This quantitative method replaces the use of autoradiography and size exclusion chromatography with combined ion-pair reversed-phase high performance liquid chromatography and in line fluorescence detection. The result of this approach is combination of speed with the generation of reproducible, high quality cDNA libraries.
我们开发了一种快速、定量的方法来分析cDNA文库制备过程中第一链合成步骤的结果,通过大小分离确定最终cDNA产物的产率和分子量范围。该方法涉及传统的cDNA文库构建,包括通常需要的所有酶促步骤,但用荧光检测取代核酸的放射性标记。分离和定量步骤均采用离子对反相高效液相色谱法(IP RP HPLC)。该定量方法采用离子对反相高效液相色谱和在线荧光检测相结合的方法,取代了放射自显影和尺寸排除色谱的使用。这种方法的结果是速度与可重复的高质量cDNA文库的生成相结合。