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PRODUCTION OF BIOTINIZED CDNA LIBRARY AND SUBSTRACTION USING THE SAME

机译:使用相同的方法生产生物素化的CDNA库并进行扣除

摘要

PURPOSE: To provide a production of cDNA library for easy and efficient subtraction using cDNA and a method for an easy subtraction using the method. ;CONSTITUTION: RNA extracted in a usual manner is annealed with poly (A) + RNA using 5'-biotin-labeled oligo dT (18 mer) as a primer and DNA is synthesized by a reverse transcriptase to obtain this biotinized cDNA library. The biotinized cDNA is hybridized with the mRNA of the cells to be subtracted, then ligated with polystyrene beads containing magnetizable substance bonded to streptavidin and the mRNA which has not been hybridized and remaining in the liquid phase is taken out to prepare the subtraction library.;COPYRIGHT: (C)1993,JPO&Japio
机译:目的:提供一种cDNA文库的生产方法,以使用cDNA进行简单而有效的扣除,以及一种使用该方法进行简单扣除的方法。 ;组成:以5'-生物素标记的oligo dT(18 mer)作为引物,将以常规方式提取的RNA与poly(A)+ RNA退火,并通过逆转录酶合成DNA,以获得该生物素化的cDNA文库。生物素化的cDNA与要减去的细胞的mRNA杂交,然后与含有与链霉亲和素结合的可磁化物质的聚苯乙烯珠连接,取出尚未杂交并保留在液相中的mRNA以制备减法文库。版权所有:(C)1993,JPO&Japio

著录项

  • 公开/公告号JPH05292971A

    专利类型

  • 公开/公告日1993-11-09

    原文格式PDF

  • 申请/专利权人 NIPPON DAINARU KK;

    申请/专利号JP19920125352

  • 发明设计人 ASADA MINORU;MIZUTANI NAGANORI;

    申请日1992-04-20

  • 分类号C12N15/10;C12Q1/68;

  • 国家 JP

  • 入库时间 2022-08-22 05:16:46

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