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出 处:《湖北大学学报(自然科学版)》2003年第2期144-147,共4页Journal of Hubei University:Natural Science
基 金:国家自然科学基金重点项目(39930100)
摘 要:为建立真核基因表达受体系统,以嗜凤梨果蝇胚胎为材料,采用常规方法获取发育4~8h的果蝇胚胎细胞,以改良M3(BF)培养液体外培养,经40d左右的原代培养后行传代培养,以后每隔7d传代一次,传至10代时按照细胞系建立标准检测细胞系的一系列生物学特性.结果显示:细胞维持体外生长将近1年,传至60代.细胞在接种的0~96h内呈指数生长,临界增殖浓度为1.0×106个(细胞) mL.部分细胞染色体呈现异倍化.经液氮冻存的细胞复苏后活性达90%以上.该细胞系是一株成功的细胞系,命名为HY-ANA.In order to establish eukaryotic gene expression system, embryos of Drosophila ananassae were used as experimental materials.Broked the embryos that had developed for 4~8 hours into cells by using conventional method, after that cultured the cells in improved M3(BF) medium in vitro. As for 40 days primary culture the cells could be passaged one time every 7 days . During this time some cells were frozen in liquid nitrogen. When the cells were passaged to 10 generation-times a series of characteristics of the cell line was examined according to the criterion of a successful cell line. Conclusion: cells were maintained in good living state for about one year, passaging to 60 generation-times. Cells proliferated at exponent from 0 hour to 96 hours after plating. The lowest concentration in which cells could proliferate was 1.0×106/mL. Parts of cells became heteroploid. The viability of the cells recovered from liquid nitrogen was up to 90% or above. The cell line was a successful cell line,named HY-ANA.
关 键 词:嗜凤梨果蝇 细胞系 生物学特性 真核基因表达受体系统 细胞培养 原代培养 传代培养
分 类 号:Q969.453.8[生物学—昆虫学] Q813.11
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