首页> 外国专利> 109 23 89 KNOCK-IN MOUSE HOMOLOGOUS RECOMBINATED BY BANK VOLE'S PRION PROTEIN GENE WHICH 109TH AMINO ACID IS METHIONINE AND FROM 23TH TO 89TH AMINO ACID CODING SEQUENCES ARE ELIMINATED AND APPLICATIONS THEREOF

109 23 89 KNOCK-IN MOUSE HOMOLOGOUS RECOMBINATED BY BANK VOLE'S PRION PROTEIN GENE WHICH 109TH AMINO ACID IS METHIONINE AND FROM 23TH TO 89TH AMINO ACID CODING SEQUENCES ARE ELIMINATED AND APPLICATIONS THEREOF

机译:109 23 89消除了109氨基酸为甲硫氨酸和23到89氨基酸编码序列的库尔氏G蛋白基因组成的敲入小鼠同源性及其应用

摘要

The present invention relates to a dissolved mouse homologous recombination with the prion protein gene of the embankment mouse, in which the 109th amino acid is methionine and the sequences encoding the 23rd to 89th amino acids, and more specifically, the 109th amino acid is methionine ( Cellular prion protein gene of bank vole from which the genes encoding amino acids 23 and 89 were removed and replaced by the knock-in homologous recombination method. A banked ratified transgenic mouse and its application technology. According to the present invention, a homologous recombination method is performed for the embankment-developed mice in which the 109th amino acid is methionine and the prion protein gene of the embankment mouse is removed from the 23rd to 89th amino acid sequence. It can be usefully used as an animal model used to evaluate the anti-prion efficacy of therapeutic candidates developed for the purpose of treating prion diseases including CJD. In addition, it can be useful to find out the role of the prion generation process or to study the performance of the anti-prion material.
机译:本发明涉及与堤防小鼠的pr病毒蛋白基因的可溶性小鼠同源重组,其中第109位氨基酸是蛋氨酸,编码第23至89位氨基酸的序列,更具体地说,第109位氨基酸是蛋氨酸(通过敲入同源重组方法去除并编码了氨基酸的23和89位氨基酸的岸田鼠细胞病毒蛋白基因,一种经批准的库藏转基因小鼠及其应用技术,根据本发明,是一种同源重组方法对堤坝发育的小鼠进行实验,其中第109个氨基酸是蛋氨酸,并且堤坝小鼠的病毒蛋白基因已从第23个至第89个氨基酸序列中删除,可用作有用的动物模型来评估抗-pr病毒治疗候选药物的功效,旨在治疗包括CJD在内的病毒疾病。 o了解the病毒生成过程的作用或研究抗-病毒材料的性能。

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