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Gene ta in order to introduce the imported gene to high efficiency gene tagetsuteingubekuta

机译:基因ta以便将导入的基因引入高效基因tagetsuteingubekuta

摘要

In the process of producing knockout mice of ZO-1 gene, we have developed a gene targeting vector for homologous recombination to occur with a high probability of 90%. As a result of examination of the optimal conditions of electroporation on epithelial cells with the targeting vector, the optimal conditions for electroporation capable of efficient gene targeting for EpH4 mouse epithelial cell line I was successful in determining the. By using the vectors of the present invention, it is possible to easily introduce the allyl ZO-1 a foreign gene for ES cells. Also, because no need to consider the impact of genomic structure also good, that the drawback of stable transformants produced when the cells and transgenic mouse production conventional can be solved is expected.
机译:在生产ZO-1基因的基因敲除小鼠的过程中,我们已经开发了一种基因靶向载体,用于同源重组,发生概率高达90%。作为用靶向载体检查上皮细胞上电穿孔的最佳条件的结果,能够有效地针对EpH4小鼠上皮细胞系I进行基因靶向的电穿孔的最佳条件成功地确定了该条件。通过使用本发明的载体,可以容易地将烯丙基ZO-1引入ES细胞的外源基因。另外,由于不需要考虑基因组结构的影响也良好,因此可以解决当可以解决常规细胞和转基因小鼠生产时产生的稳定转化子的缺点。

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