首页> 外国专利> CDNA CLONE OF POST-TRANSFUSION NON-A NON-B HEPATITIS VIRUS (NANB) AND USE THEREOF

CDNA CLONE OF POST-TRANSFUSION NON-A NON-B HEPATITIS VIRUS (NANB) AND USE THEREOF

机译:输血后非甲非乙型肝炎病毒(NANB)的CDNA克隆及其用途

摘要

NEW MATERIAL:A cDNA clone such as phage clone YS1 or phage clone YS2 containing a nucleotide of about 5.4Kb coding the amino acid sequence of a post-transfusion non-A non-B hepatitis virus (NANB) and prepared by adding an EcoRI linker to a duplex cDNA fragment prepared by using a template consisting of a refined RNA existing in a particle fraction separated from serum and substituting and inserting the addition product to an EcoRI site of a lambda gt10 vector. USE:Agent for the diagnosis, prevention and remedy of non-A non-B hepatitis. Blood cleaning agent for transfusion. PREPARATION:The objective cDNA clone can be prepared e.g. by adding 20% polyethylene glycol to a plasma originated from a non-A non-B hepatitis patient, centrifuging the mixture at a high speed, solubilizing the precipitate with TEN buffer solution, etc., centrifuging at a high speed to collect purified RNA, preparing a duplex cDNA using the RNA as a template, adding an EcoRI linker to the cDNA and substituting and inserting the addition product to the EcoRI site of a lambda gt10 vector.
机译:新材料:一种cDNA克隆,例如噬菌体克隆YS1或噬菌体克隆YS2,其包含约5.4Kb的核苷酸,编码输血后非A非B非乙型肝炎病毒(NANB)的氨基酸序列,并通过添加EcoRI接头制备通过使用模板制备双链cDNA片段,该模板通过使用由存在于与血清分离的颗粒级分中的精制RNA组成的模板制成,并将加成产物取代并插入λgt10载体的EcoRI位点。用途:用于诊断,预防和治疗非甲型非乙型肝炎的药物。输血用血液清洁剂。制备:可以制备目的cDNA克隆,例如。通过向来自非A非B型肝炎患者的血浆中添加20%聚乙二醇,高速离心混合物,用TEN缓冲溶液等溶解沉淀物,高速离心以收集纯化的RNA,使用RNA作为模板制备双链cDNA,将EcoRI接头添加到cDNA,并将添加产物取代并插入到λgt10载体的EcoRI位点。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号