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Screening of the Sf900-II SFM insect cell culture medium and recombinant baculovirus for the expression of recombinant human transferrin

机译:筛选用于表达重组人转铁蛋白的Sf900-II SFM昆虫细胞培养基和重组杆状病毒

摘要

Optimized medium composition and high purity recombinant baculovirus stock have historically contributed to high yield recombinant protein expressed in the insect cells baculovirus expression system. In achieving this, screening experiments were conducted to identify the recombinant baculovirus and medium components in Sf900-II SFM that gave significant production of recombinant human transferrin (rhTf). For medium screening, a Plackett-Burman screening experiments were conducted. For recombinant baculovirus screenings, an end point dilution method based on Poisson distribution was used. RhTf was analyzed using SDS-PAGE and ELISA while the software Statistica (Statsoft, v. 5.0) was used to analyze the results obtained. The results show that glucose and glutamine had the most effect with more than 95% significance, while the recombinant baculovirus was identified at 98.7% purity. The two screening methods were very useful to rapidly screen recombinant baculovirus and culture medium. At the same time, the recombinant protein yield was increased to ~20 ug/ml.
机译:历史上,优化的培养基组成和高纯度重组杆状病毒原种有助于在昆虫细胞杆状病毒表达系统中表达高产量的重组蛋白。为了实现这一目标,进行了筛选实验,以鉴定重组杆状病毒和Sf900-II SFM中的培养基成分,该重组杆状病毒和培养基成分可大量生产重组人转铁蛋白(rhTf)。对于培养基筛选,进行了Plackett-Burman筛选实验。对于重组杆状病毒筛选,使用基于泊松分布的终点稀释方法。使用SDS-PAGE和ELISA分析RhTf,同时使用Statistica软件(Statsoft,v。5.0)分析所得结果。结果表明,葡萄糖和谷氨酰胺具有最大的作用,意义超过95%,而重组杆状病毒的纯度为98.7%。两种筛选方法对于快速筛选重组杆状病毒和培养基非常有用。同时,重组蛋白产量增加到〜20 ug / ml。

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