• 结论原核表达系统有效克隆较高纯度CHM - I基因。

    Conclusion The more effective CHM-I clone with high purity could be expressed by procaryotic expression system.

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  • 方法原核表达系统高效表达重组3病毒六邻体蛋白

    Methods Under the optimum expression conditions, the hexon protein of human type 3 adenovirus was efficiently expressed in e.

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  • 目的构建凋亡原核表达系统,以制备物质凋亡素融合蛋白

    Objective to construct an apoptin expression system to produce an antigen, apoptin fusion protein.

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  • 目的建立HPV16 L 1蛋白表达系统纯化方法纯化目的蛋白。

    Objective To establish a method of purification of HPV16L1 protein expressed in a prokaryotic system and obtain the purified protein.

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  • 本研究成功利用表达系统实现了CTNY-ESO-1的可溶性表达

    So human CT antigen NY-ESO-1 could be successfully expressed in prokaryotic expression system.

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  • 结果HPV16L1蛋白原核表达系统以不溶性包涵形式存在,通过方法可以获得纯化的蛋白。

    Results HPV16L1 proteins formed inclusion bodies in bacterial expression system, this assay could purified HPV16L1 proteins.

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  • 实验成功构建CHIPS蛋白表达系统CHIPS免疫研究蛋白的其他功能研究奠定基础

    The successful construction of the CHIPS protein's prokaryotic expression system in this study has laid a foundation for further study on the protein's immunogenicity and other functions.

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  • 通过基因克隆等方法,选择表达系统对目的蛋白进行分离纯化,初步获得活性人内毒素结合肽ebp

    We isolated and purified EBP effectively, and obtained EBP with biological activity for the first time with gene cloning method and prokaryotic expression system.

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  • 尽管研究者细胞表达系统对胸腺肽表达进行了研究,但由于原核表达系统缺乏翻译加工修饰等缺点,限制了应用

    Although the thymosin has been successfully expressed in the prokaryotic cell system, its application is restricted because of its deficiency of modification after translation.

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  • 蛋白质磷酸化去磷酸化作为原核细胞表达调控关键环节,了解其对功能影响可以深入理解生命系统分子水平的调控状况

    As the key point of expression modulation in prokaryotic and eukaryotic cells, the protein phosphorylation and dephosphorylation may help reveal the status of the life system at the molecular level.

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  • 研究目的是分子设计构建G-CSF单体分子具有半衰期更长、生物活性更高的新型重组人G-CSF/G-CSF双体分子(简称G-G),并原核系统进行高效表达

    Molecule design, construction and high level expression in E. coli. of bimolecular G-CSF with longer half life and higher bioactivities than single molecular G-CSF.

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  • 酵母菌乙醇脱氢乙醛脱氢酶之抽取及其原核系统表达

    Extraction of Alcohol Dehydrogenase and Aldehyde Dehydrogenase from Saccharomyces cerevisiae and their Expression by Prokaryotic System...

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  • 酵母菌乙醇脱氢乙醛脱氢酶之抽取及其原核系统表达

    Extraction of Alcohol Dehydrogenase and Aldehyde Dehydrogenase from Saccharomyces cerevisiae and their Expression by Prokaryotic System...

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