首页> 外国专利> A procedure to produce a complementary DNA clonadoo its modified DNA that encodes a polypeptide of factor denecrosis Tumors

A procedure to produce a complementary DNA clonadoo its modified DNA that encodes a polypeptide of factor denecrosis Tumors

机译:产生互补DNA克隆的过程,其修饰的DNA编码因子坏死因子多肽

摘要

Procedure to produce a cloned complementary DNA or modified DNA that encodes a polypeptide of tumor necrosis factor.Includes: (a) cultivating Rabbit macrophages with inducers; b) Separating a fraction containing a Messenger RNA (mRNA) of Rabbit Tumor Necrosis Factor of cultivation of macrophages; c) treating the mRNA with reverse transcriptase.For a Single Stranded complementary DNA (cDNA); (d) to convert the Single Stranded cDNA in a double stranded cDNA; (e) The Double stranded cDNA INSERT IN Plasmid vector; (f) to introduce recombinant Plasmid in a host to transform and build a double stranded cDNA Cdna library; and G hybridize to cdna library to obtain cDNA encoding factorRabbit tumor necrosis.
机译:产生编码肿瘤坏死因子多肽的克隆互补DNA或修饰DNA的程序,包括:(a)用诱导剂培养兔巨噬细胞; b)分离含有巨噬细胞培养的兔肿瘤坏死因子信使RNA(mRNA)的级分; c)用逆转录酶处理mRNA。对于单链互补DNA(cDNA); (d)将单链cDNA转化成双链cDNA; (e)双链cDNA INSERT IN质粒载体; (f)将重组质粒引入宿主中以转化并建立双链cDNA Cdna文库; G与cdna文库杂交,获得编码因子兔肿瘤坏死的cDNA。

著录项

  • 公开/公告号ES8605578A1

    专利类型

  • 公开/公告日1986-09-01

    原文格式PDF

  • 申请/专利权人 DAINIPPON PHARMACEUTICAL CO.LTD.;

    申请/专利号ES19850547436

  • 发明设计人

    申请日1985-09-30

  • 分类号C12N15/00;A61K37/02;

  • 国家 ES

  • 入库时间 2022-08-22 07:37:33

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