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    • 3. 发明授权
    • Method for increasing the efficiency of inducing pluripotent stem cells
    • 提高多能干细胞诱导效率的方法
    • US09163217B2
    • 2015-10-20
    • US13808596
    • 2012-03-31
    • Duanqing PeiTao Wang
    • Duanqing PeiTao Wang
    • C12N15/00C12N5/0775C12N5/074
    • C12N5/0662C12N5/0696C12N2500/38C12N2501/602C12N2501/72C12N2506/13C12N2510/00
    • The present invention relates to a method for increasing the efficiency of inducing pluripotent stem cells by utilizing genes Jhdm1b and Jhdm1a that modify histone. By utilizing Jhdm1b, Jhdm1a, and a stem cell inducing factor, the present invention increases the efficiency of inducing pluripotent stem cells and increases the quality of induced pluripotent stem cells. The stem cell inducing factor is a combination of Oct4 and Klf4, or a combination of Sox2, Oct4, and Klf4, or a combination of Oct4 and Sox2, and Oct4 alone. The method further comprises exposing the cells to vitamin C, which further increases the efficiency of inducing pluripotent stem cells as compared with the case where no vitamin C is used. By using less stem cell reducing factors, the method of the present invention reduces the potential carcinogenicity, obtains a high inducing efficiency, and provides high-quality induced pluripotent stem cells capable of germ-line transmission.
    • 本发明涉及通过使用修饰组蛋白的基因Jhdm1b和Jhdm1a来提高诱导多能干细胞的效率的方法。 通过利用Jhdm1b,Jhdm1a和干细胞诱导因子,本发明增加诱导多能干细胞的效率并增加诱导多能干细胞的质量。 干细胞诱导因子是Oct4和Klf4的组合,或Sox2,Oct4和Klf4的组合,或Oct4和Sox2以及Oct4的组合。 该方法还包括将细胞暴露于维生素C,与不使用维生素C的情况相比,这进一步增加诱导多能干细胞的效率。 通过使用较少的干细胞减少因子,本发明的方法降低潜在致癌性,获得高诱导效率,并提供能够进行种系传播的高质量诱导多能干细胞。
    • 5. 发明申请
    • METHOD FOR INCREASING THE EFFICIENCY OF INDUCING PLURIPOTENT STEM CELLS
    • 增加诱导大脑干细胞效率的方法
    • US20130302893A1
    • 2013-11-14
    • US13808596
    • 2012-03-31
    • Duanqing PeiTao Wang
    • Duanqing PeiTao Wang
    • C12N5/0775
    • C12N5/0662C12N5/0696C12N2500/38C12N2501/602C12N2501/72C12N2506/13C12N2510/00
    • The present invention relates to a method for increasing the efficiency of inducing pluripotent stem cells, and more particularly, to a method for increasing the efficiency of inducing pluripotent stem cells by utilizing genes Jhdm1b and Jhdm1a that modify histone. By utilizing Jhdm1b, Jhdm1a, and a stem cell inducing factor, the present invention increases the efficiency of inducing pluripotent stem cells and increases the quality of induced pluripotent stem cells. The stem cell inducing factor is a combination of Oct4 and Klf4, or a combination of Sox2, Oct4, and Klf4, or a combination of Oct4 and Sox2, and Oct4 alone. The method of the present invention further comprises exposing the cells to vitamin C, which further increases the efficiency of inducing pluripotent stem cells as compared with the case where no vitamin C is used. By using less stem cell reducing factors, the method of the present invention reduces the potential carcinogenicity, obtains a high inducing efficiency, and provides high-quality induced pluripotent stem cells capable of germ-line transmission.
    • 本发明涉及提高多能干细胞诱导效率的方法,更具体地说,涉及通过利用修饰组蛋白的基因Jhdm1b和Jhdm1a来提高诱导多能干细胞的效率的方法。 通过利用Jhdm1b,Jhdm1a和干细胞诱导因子,本发明增加诱导多能干细胞的效率并增加诱导多能干细胞的质量。 干细胞诱导因子是Oct4和Klf4的组合,或Sox2,Oct4和Klf4的组合,或Oct4和Sox2以及Oct4的组合。 本发明的方法还包括将细胞暴露于维生素C,与不使用维生素C的情况相比,这进一步增加诱导多能干细胞的效率。 通过使用较少的干细胞减少因子,本发明的方法降低潜在致癌性,获得高诱导效率,并提供能够进行种系传播的高质量诱导多能干细胞。
    • 8. 发明申请
    • CULTURE MEDIUM SUPPLEMENT AND USE THEREOF
    • 文化媒介补充及其使用
    • US20130040390A1
    • 2013-02-14
    • US13263865
    • 2010-07-29
    • Duanqing PeiJiekai ChenJing Liu
    • Duanqing PeiJiekai ChenJing Liu
    • C12N5/071
    • C12N5/0696C12N2500/38C12N2500/90C12N2501/11C12N2501/115C12N2501/33C12N2501/603C12N2501/727C12N2501/999C12N2506/1307C12N2510/00
    • The present invention provides a chemically defined culture system, by which induced pluripotent stem (iPS) cells are obtained with high efficiency. The culture medium supplement of the present invention includes vitamin C and a glycogen synthase kinase-3 inhibitor; another culture medium supplement of the present invention further includes, in addition to vitamin C and the glycogen synthase kinase-3 inhibitor, vitamin B12, insulin, a receptor tyrosine kinase, and an anti-oxidant; and the culture medium supplement of the present invention may further be a mixture of the above two culture medium supplements with a serum replacement cell growth promoter. The present invention further provides a complete culture medium for iPS cells, which is formed by one or more of a basal culture medium, serum, and a serum replacement supplement, and the above culture medium supplements, or formed only by the above culture medium supplements and a basal culture medium. The culture system of the present invention is a chemically defined culture system free of serum and contamination from animal source, by which the iPS cells are obtained with high efficiency. The culture system maintains the growth and proliferation of the cells in conversion of somatic cells to iPS cells in absence of feeder cells, significantly accelerates the iPS cell induction process, and greatly improves the induction efficiency of somatic cells into iPS cells.
    • 本发明提供一种化学上定义的培养系统,通过该培养系统以高效率获得诱导的多能干细胞(iPS)细胞。 本发明的培养基补充剂包括维生素C和糖原合酶激酶-3抑制剂; 除了维生素C和糖原合酶激酶-3抑制剂之外,本发明的另一种培养基补充剂还包括维生素B12,胰岛素,受体酪氨酸激酶和抗氧化剂; 并且本发明的培养基补充物还可以是上述两种培养基补充物与血清替代细胞生长促进剂的混合物。 本发明还提供一种用于iPS细胞的完整培养基,其由一种或多种基础培养基,血清和血清替代物补充剂形成,并且上述培养基补充剂或仅由上述培养基补充剂形成 和基础培养基。 本发明的培养系统是不含动物源的血清和污染的化学上定义的培养系统,通过该培养系统以高效率获得iPS细胞。 培养体系保持细胞在不存在饲养细胞时体细胞转化为iPS细胞的生长和增殖,显着加速iPS细胞诱导过程,并大大提高体细胞诱导iPS细胞的诱导效率。