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首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Screening of single-cell clonal lines fromPapilio demoleusLinnaeus cell lines for exogenous protein expression and adaptation in serum-free culture
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Screening of single-cell clonal lines fromPapilio demoleusLinnaeus cell lines for exogenous protein expression and adaptation in serum-free culture

机译:筛选单细胞克隆物系FRFPAPILIO Demoleluslinnaeus细胞系进行外源蛋白表达和血清培养物的适应

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摘要

In this paper, four established cell lines derived from newly hatched larvae ofPapilio demoleusLinnaeus and 57 single-cell clones derived from the 3 lines were used as test materials. Recombinant beta-galactosidase baculovirus AcMNPV-Gal was used to infect theP. demoleusL. cell lines and the single-cell clones, and recombinant protein expression in each cell line was detected and compared. Three clonal cell lines, RIRI-PaDe-1-C1, RIRI-PaDe-2-C6 and RIRI-PaDe-3-C52, which showed significantly higher beta-galactosidase expression levels than those of the parental cell lines, were selected. Five types of commercial serum-free media for insect cells, Express Five SFM, Ex-Cell 405, Sf-900III SFM, Sf-900II SFM and HyClone Serum-Free Media, were used to adapt RIRI-PaDe-2-C6 cells and RIRI-PaDe-3-C52 cells to serum-free culture conditions, and the growth characteristics of the cells and the exogenous protein expression characteristics before and after adaptation were compared. The results showed that RIRI-PaDe-2-C6 cells could stably proliferate in Ex-Cell 405, RIRI-PaDe-3-C52 cells could stably proliferate in Express Five SFM and Ex-Cell 405, and the rate of proliferation of and the level of expression of beta-galactosidase in RIRI-PaDe-3-C52 cells were significantly increased in Express Five SFM.
机译:在本文中,使用了衍生自新阴影幼虫的四种成熟的细胞系,其普及探测器林和57个单细胞克隆衍生自3系衍生自3系的单细胞克隆。重组β-半乳糖苷酶Baculovirus Acmnpv-Gal被用来感染PP。 Demoleusl。检测细胞系和单细胞克隆,并进行比较各细胞系中的重组蛋白表达。选择了三种克隆细胞系,RIRI-PADE-1-C1,RIRI-PADE-2-C6和RIRI-PADE-3-C52,其显示出明显更高的β-半乳糖苷酶表达水平,而不是亲本细胞系。用于昆虫细胞的五种类型的商用血清培养基,表达五SFM,外池405,SF-900III SFM,SF-900II SFM和Hyclone无血清培养基,用于适应Riri-Pade-2-C6细胞和RIRI-PADE-3-C52细胞对无血清培养条件,并比较了适应前后细胞的生长特性和外源蛋白表达特征。结果表明,在外细胞405中可以稳定地增殖RIRI-PADE-2-C6细胞,RIRI-PADE-3-C52细胞可以在表达五SFM和前细胞405中稳定增殖,以及和增殖速率表达五SFM明显增加了β-半乳糖苷酶的表达水平。

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