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Vectors and methods for making such vectors and for expressive cloned genes

机译:载体和制备此类载体以及表达性克隆基因的方法

摘要

Improved vectors and methods for expressing cloned genes of prokaryotic or eukaryotic origin and methods of making such vectors are disclosed, the improved vectors comprising promoters and operators from . lambda. phages and preferably do not include an active cro gene or an active N gene, the vectors having at least one endonuclease recognition site for cloning desired genes less than about 300 base pairs from the promoters and operators and being useful, as are methods utilizing the vectors, in producing a wide variety of prokaryotic, eukaryotic and viral polypeptides, hormones, enzymes, antigens, proteins and amino acids.
机译:公开了用于表达原核或真核来源的克隆基因的改进的载体和方法,以及制备这种载体的方法,所述改进的载体包含来自的启动子和操纵子。 lambda。噬菌体,并且优选地不包括活性cro基因或活性N基因,载体具有至少一个核酸内切酶识别位点,用于从启动子和操纵子克隆少于约300个碱基对的所需基因,并且与利用载体的方法一样有用在生产各种各样的原核,真核和病毒多肽,激素,酶,抗原,蛋白质和氨基酸方面。

著录项

  • 公开/公告号US4874702A

    专利类型

  • 公开/公告日1989-10-17

    原文格式PDF

  • 申请/专利权人 BIOGEN INC.;

    申请/专利号US19860921803

  • 发明设计人 WALTER C. FIERS;RENE ERIK REMAUT;

    申请日1986-10-20

  • 分类号C12N15/00;C12N1/20;C12P21/00;

  • 国家 US

  • 入库时间 2022-08-22 06:27:20

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