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    • 64. 发明公开
    • METHOD FOR INTRODUCING NUCLEIC ACIDS INTO A CELL
    • 将核酸引入细胞的方法
    • EP3241905A1
    • 2017-11-08
    • EP16168589.6
    • 2016-05-06
    • Miltenyi Biotec GmbH
    • JURK, MarionWILD, StefanBOSIO, Andreas
    • C12N15/87
    • C12N15/87C07K14/4703
    • The present invention provides the use of a nucleic acid encoding SOCS 1 for enhancing the efficacy of introducing at least one nucleic acid of interest into a cell; a method of repeated transfection of a cell with at least one nucleic acid of interest comprising the steps of adding
      a) nucleic acid encoding SOCS1, and simultaneously or subsequently b) at least one nucleic acid of interest encoding at least one polypeptide of interest, wherein at least step b) is repeated at least once; and a method of electroporation of a cell with at least one nucleic acid of interest comprising the steps of adding to the cell a) a nucleic acid encoding SOCS1, and simultaneously or subsequently b) said at least one nucleic of interest. The at least one nucleic acid of interest and the nucleic acid encoding SOCS 1 may be mRNAs, wherein each of said mRNAs has a poly(A) tail at its 3'end comprising at least 200 adenines.
    • 本发明提供编码SOCS1的核酸用于增强将至少一种感兴趣的核酸导入细胞的功效的用途; 用至少一种目标核酸重复转染细胞的方法,包括以下步骤:添加a)编码SOCS1的核酸,并且同时或随后b)编码至少一种目的多肽的至少一种感兴趣的核酸,其中 至少步骤b)重复至少一次; 以及用至少一种感兴趣的核酸对细胞进行电穿孔的方法,所述方法包括以下步骤:向细胞中加入a)编码SOCS1的核酸,并且同时或随后b)所述至少一种感兴趣的核酸。 所述至少一种目的核酸和编码SOCS1的核酸可以是mRNA,其中每种所述mRNA在其3'末端具有包含至少200个腺嘌呤的聚(A)尾。
    • 66. 发明公开
    • METHOD FOR NATURAL KILLER CELL EXPANSION
    • VERFAHRENFÜRNATÜRLICHEKILLERZELLENEXPANSION
    • EP3138905A1
    • 2017-03-08
    • EP15183968.5
    • 2015-09-04
    • Miltenyi Biotec GmbH
    • GRANZIN, MarkusHUPPERT, Volker
    • C12N5/0783
    • C12N5/0646C12N2501/2302C12N2501/2315C12N2501/2321
    • The present invention provides a method for in-vitro culturing and expanding natural killer (NK) cells in a cell culture medium comprising a population of NK cells, the method comprising a) adding an effective concentration of interleukin-21 (IL-21) at the beginning of the culturing process to said medium, b) adding repeatedly an effective concentration of interleukin-2 (IL-2) and/or interleukin-15 (IL-15) to said medium, and c) adding repeatedly feeder cells or membrane particles thereof to said medium, wherein said feeder cells are B cell derived which are EBV immortalized; and wherein said expansion of NK cells in said cell culture medium is maintained for at least 3 weeks.
    • 本发明提供了在包含NK细胞群的细胞培养基中体外培养和扩增天然杀伤(NK)细胞的方法,所述方法包括:a)将有效浓度的白细胞介素-21(IL-21)加入到 培养过程开始于所述培养基,b)向所述培养基反复加入白细胞介素-2(IL-2)和/或白细胞介素-15(IL-15)的有效浓度,c)重复加入饲养细胞或膜 其中所述饲养细胞是B细胞衍生的,其是EBV永生化的; 并且其中所述细胞培养基中NK细胞的所述扩增保持至少3周。