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机构地区:[1]南京农业大学作物遗传与种质创新国家重点实验室/农业部南方蔬菜遗传改良重点开放实验室,江苏南京210095
出 处:《南京农业大学学报》2012年第1期14-20,共7页Journal of Nanjing Agricultural University
基 金:国家973计划项目(2009CB119001-04);教育部新世纪优秀人才支持计划项目(NCET-07-0439)
摘 要:以不结球白菜品种‘矮脚黄’的雌蕊为材料,从蛋白质提取、IEF程序、IPG胶条pH范围和染色方法等方面进行比较,利用Tris-HCl提取方法,使用pH 4~7 IPG胶条和改进的等电聚焦程序,改良银染方法,建立了适用于不结球白菜雌蕊蛋白质的双向电泳技术体系,并使用该体系对开花前2 d的花蕾雌蕊和开花2 d后的雌蕊蛋白质进行比较分析,获得187个差异蛋白点。To establish a proper two-dimensional gel electrophoresis(2-DE) system for pistils of Brassica campestris ssp.chinensis Makino,several protein extraction methods,isoelectric focusing procedures and silver staining methods were compared.Consequently,the total proteins were extracted from non-heading Chinese cabbage’Aijiaohuang’pistils by the tris(hydroxymethyl)aminomethane-hydrochloric acid(Tris-HCl)extraction method.The proteins were separated by a improved isoelectric focusing procedure,with 17 cm,pH 4-7 IPG strips and the 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis(SDS-PAGE).The 2-DE map was dyed by the improved silver staining method.The different protein expression by the previous established protocol between bud pistils 2 days before florescence and blossom pistils 2 days after florescence was compared,and 187 distinct protein spots were detected.
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