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    • 4. 发明公开
    • METHOD FOR SMALL RNA ISOLATION
    • 小RNA分离方法
    • EP2324131A1
    • 2011-05-25
    • EP09815159.0
    • 2009-09-17
    • GE Healthcare Bio-Sciences Corp.
    • DHULIPALA, RohiniCAI, Yuyang ChristineJIANG, MiaoDAR, Mubasher
    • C12Q1/68C07H21/02
    • C12N15/111C12N15/1006C12N2310/141C12N2330/10
    • This invention relates to a simple and rapid method for the extraction and purification of small RNA from a sample solution. Accordingly, a sample is first mixed with an organic solvent to form a mixture containing the solvent. The mixture is applied to a first mineral support for large RNA to bind. The filtrate is collected which contain unbound small RNA, and is mixed with a second organic solvent to form a second mixture containing the second solvent. This second mixture is applied to a second mineral support for small RNA to bind. After a wash step, the small RNA is eluted. Also provided is a method for the isolation of large RNA, by eluting the large RNA from the first mineral support. In addition, total protein is present in the filtrate and can be isolated by a conventional method.
    • 本发明涉及从样品溶液中提取和纯化小RNA的简单而快速的方法。 因此,首先将样品与有机溶剂混合以形成含有溶剂的混合物。 将混合物施加到第一种矿物质载体上以结合大RNA。 收集含有未结合的小RNA的滤液,并将其与第二有机溶剂混合以形成含第二溶剂的第二混合物。 将第二种混合物应用于第二种矿物支持物以结合小RNA。 洗涤步骤后,小RNA被洗脱。 还提供了通过从第一种矿物质载体上洗脱大RNA来分离大RNA的方法。 另外,总蛋白质存在于滤液中并且可以通过常规方法分离。