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    • 5. 发明申请
    • STABLE DIFFERENTIATION OF ADULT STEM CELLS
    • 成熟干细胞的稳定分化
    • US20080160614A1
    • 2008-07-03
    • US11966427
    • 2007-12-28
    • Samuel SaportaElise SpencerRania Shamekh
    • Samuel SaportaElise SpencerRania Shamekh
    • C12N5/02C12N5/00
    • C12N5/0619C12N2506/02C12N2533/32
    • A method of differentiating adult stem cells, such as those derived from a teratocarcinoma cell line, the Ntera2/D1 clone (NT2). The developed cells exhibit a stable neurotransmitter phenotype without the required use of growth factors or retinoic acid in differentiation process, which may be difficult to completely remove during commercial production. An identification of specific neurotransmitters is possible in these differentiated NT2-derived neurons (NT2-N) after 30 days in culture or 30 days survival in vivo. The invention includes a method to stably differentiate neuronal stem/precursor cells to a neuronal phenotype for use in cell replacement therapy for neurodegenerative disease, stroke or spinal cord injury. At least four different types of neurons are produced from this method of differentiation: dopaminergic, cholinergic, GABAergic and glutaminergic. Additionally, since the cells are a cancer stem cell prior to differentiation, they may serve as a model system for developing anti-cancer therapies aimed at the cancer stem cell, rather than the more differentiated daughter cell.
    • 一种区分成体干细胞的方法,例如衍生自畸胎癌细胞系的那些,Ntera2 / D1克隆(NT2)。 发育的细胞在分化过程中不需要使用生长因子或视黄酸,表现出稳定的神经递质表型,这在商业生产过程中可能难以完全去除。 在培养30天后,在体内存活30天,这些分化的NT2来源的神经元(NT2-N)可以鉴定特异性神经递质。 本发明包括将神经元干/前体细胞稳定地分化为用于神经变性疾病,中风或脊髓损伤的细胞替代疗法中的神经元表型的方法。 从这种分化方法产生至少四种不同类型的神经元:多巴胺能,胆碱能,GABA能和谷氨酸能。 此外,由于细胞是分化前的癌干细胞,它们可以用作开发针对癌症干细胞的抗癌疗法的模型系统,而不是更加分化的子细胞。
    • 6. 发明授权
    • Stable differentiation of NT2 cells
    • NT2细胞稳定分化
    • US08778680B2
    • 2014-07-15
    • US11966427
    • 2007-12-28
    • Samuel SaportaElise SpencerRania Shamekh
    • Samuel SaportaElise SpencerRania Shamekh
    • A61K35/30G01N33/48
    • C12N5/0619C12N2506/02C12N2533/32
    • A method of differentiating adult stem cells, such as those derived from a teratocarcinoma cell line, the Ntera2/D1 clone (NT2). The developed cells exhibit a stable neurotransmitter phenotype without the required use of growth factors or retinoic acid in differentiation process, which may be difficult to completely remove during commercial production. An identification of specific neurotransmitters is possible in these differentiated NT2-derived neurons (NT2-N) after 30 days in culture or 30 days survival in vivo. The invention includes a method to stably differentiate neuronal stem/precursor cells to a neuronal phenotype for use in cell replacement therapy for neurodegenerative disease, stroke or spinal cord injury. At least four different types of neurons are produced from this method of differentiation: dopaminergic, cholinergic, GABAergic and glutaminergic. Additionally, since the cells are a cancer stem cell prior to differentiation, they may serve as a model system for developing anti-cancer therapies aimed at the cancer stem cell, rather than the more differentiated daughter cell.
    • 一种区分成体干细胞的方法,例如衍生自畸胎癌细胞系的那些,Ntera2 / D1克隆(NT2)。 发育的细胞在分化过程中不需要使用生长因子或视黄酸,表现出稳定的神经递质表型,这在商业生产过程中可能难以完全去除。 在培养30天后,在体内存活30天,这些分化的NT2来源的神经元(NT2-N)可以鉴定特异性神经递质。 本发明包括将神经元干/前体细胞稳定地分化为用于神经变性疾病,中风或脊髓损伤的细胞替代疗法中的神经元表型的方法。 从这种分化方法产生至少四种不同类型的神经元:多巴胺能,胆碱能,GABA能和谷氨酸能。 此外,由于细胞是分化前的癌干细胞,它们可以用作开发针对癌症干细胞的抗癌疗法的模型系统,而不是更加分化的子细胞。