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    • 23. 发明申请
    • METHOD FOR PREPARING SPECIFIC CELLS OF HUMAN-DERIVED CELLS
    • 用于制备人源细胞特异性细胞的方法
    • US20150259703A1
    • 2015-09-17
    • US14434284
    • 2013-02-05
    • TRDIGM & CO., LTD.
    • Katsutomo Hamada
    • C12N15/85C12N9/14G01N33/50C12N9/12
    • C12N15/85C12N9/1276C12N9/14C12N15/11C12N2330/10C12N2503/02C12N2510/00C12N2510/04C12N2800/90C12Y207/07049C12Y306/01003G01N33/5011
    • A method for preparing neoplastically transformed cells from human-derived cells, including the step of introducing human telomerase catalytic subunit (hTERT) gene, SV40 small T antigen (SV40ST) gene, and an oligonucleotide derived from Alu7 sequence into the human-derived cells. A method for introducing a gene for neoplastically transforming human-derived cells, including incorporating human telomerase catalytic subunit (hTERT) gene, SV40 small T antigen (SV40ST) gene, and an oligonucleotide derived from Alu7 sequence into the same or different vectors, and introducing the genes into human-derived cells therewith. The methods of the present invention can be utilized upon induction of neoplastic transformation to various human normal cells in order to elucidate mechanisms for onset of cancer, so that the method can be effectively utilized in the search of a new drug discovery target molecule.
    • 包括将人端粒酶催化亚基(hTERT)基因,SV40小T抗原(SV40ST)基因导入人源性细胞的衍生细胞的方法,以及衍生自Alu7序列的寡核苷酸引入人源细胞的步骤。 引入人源性细胞的新型基因导入方法,包括将人端粒酶催化亚基(hTERT)基因,SV40小T抗原(SV40ST)基因以及衍生自Alu7序列的寡核苷酸引入相同或不同的载体中,并引入 将基因转化成人源细胞。 本发明的方法可以在诱导对各种人正常细胞的肿瘤转化时使用,以阐明癌症发病的机制,从而可以有效地利用该方法来寻找新的药物发现靶分子。