首页> 外国专利> RECOMBINANT PLASMID DNA PFASTBAC-G2R COMPRISING SMALLPOX VIRUS GENOME FRAGMENT ENCODING PROTEIN-ANALOG OF TUMOR NECROSIS FACTOR RECEPTOR AND STRAIN OF BACULOVIRUS BTRI67 PRODUCING SOLUBLE RECEPTOR OF SMALLPOX VIRUS TUMOR NECROSIS FACTOR

RECOMBINANT PLASMID DNA PFASTBAC-G2R COMPRISING SMALLPOX VIRUS GENOME FRAGMENT ENCODING PROTEIN-ANALOG OF TUMOR NECROSIS FACTOR RECEPTOR AND STRAIN OF BACULOVIRUS BTRI67 PRODUCING SOLUBLE RECEPTOR OF SMALLPOX VIRUS TUMOR NECROSIS FACTOR

机译:包含鼠痘病毒基因组片段的重组质粒DNA PFASTBAC-G2R编码蛋白-类似肿瘤坏死因子受体和杆状病毒BTRI67的可溶性菌株,产生鼠痘病毒肿瘤坏死因子。

摘要

FIELD: genetic engineering, molecular biology, biotechnology.;SUBSTANCE: method involves using polymerase chain reaction (PCR) method for isolating gene G2R encoding the protein-analog of human tumor necrosis factor-alpha receptor from the smallpox virus genome of the strain "India-1967". Then this gene is cloned in donor plasmid pFastBac and the recombinant bacmid is reconstructed by site-specific transposition method. Method involves transfection of insect cells with recombinant bacmide for generation of recombinant baculovirus BTRi67 expressing gene G2R in the insect cell line Sf21. Invention provides the high level of synthesis of the end product and its correct post-translation modification. Invention can be used for preparing a medicinal agent of the new generation used for control of human severe diseases associated with hyperproduction of tumor necrosis factor-alpha (TNF-alpha).;EFFECT: valuable biological and medicinal properties of plasmid and strain.;3 cl, 3 dwg, 6 ex
机译:领域:基因工程,分子生物学,生物技术。;研究方向:该方法涉及使用聚合酶链反应(PCR)方法从菌株“印度”的天花病毒基因组中分离编码人肿瘤坏死因子-α受体蛋白类似物的基因G2R。 -1967”。然后将该基因克隆到供体质粒pFastBac中,并通过位点特异性转座方法重建重组杆粒。该方法涉及用重组巴米德转染昆虫细胞以在昆虫细胞系Sf21中产生表达杆状病毒BTRi67的表达基因G2R。本发明提供了最终产物的高水平合成及其正确的翻译后修饰。本发明可用于制备用于控制与肿瘤坏死因子-α(TNF-α)过量产生有关的人类严重疾病的新一代药物。效果:质粒和菌株的有价值的生物学和医学特性; 3 cl,3 dwg,6 ex

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