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    Large-scale Production of Plasmid DNA
    质粒DNA的大规模制备
    Large-scale fabrication and magnetic properties of Ni_(80) Fe_(20) nanowire arrays
    大规模制备Ni_(80)Fe_(20)纳米线阵列及其磁学特性研究
    Comparison of large-scale preparation of recombinant human BMP-4 and BMP-2 mature peptide expressed in E.coli
    大肠杆菌表达的重组人BMP-2和hBMP-4成熟肽大规模制备方法的比较
    The Large Scale Preparation of Recombinant Human Bone Morphogenetic Protein-4 Mature Peptide
    重组人骨形成蛋白-4的大规模制备
    Analysis of Using Urea in Large-scale Purification of rhBMP-2m Expressed from E.coli
    rhBMP-2m大规模制备纯化过程中使用尿素的分析
    Large-scale Plasmid DNA Preparation by Flow-Through Thermal Lysis
    连续热裂解法大规模制备质粒DNA
    However, researcch was concentrated on the chiral analysis and chiral recognition mechanism, and the study on the preparative separation is not excessive.
    手性色谱拆分法是发展较快的一种手性分离方法,但目前研究侧重于手性药物的分析与手性识别机理研究,大规模制备的应用研究还很少。
    However, research was concentrated on the chiral analysis and chiral recognition mechanism, and the study on the preparative separation is not excessive.
    手性色谱拆分法是发展较快的一种手性分离方法,但目前研究侧重于手性药物的分析与手性识别机理研究,大规模制备的应用研究还很少。
    pUDK-HGF has been submitted to Chinese SFDA for clinic trails.
    一、质粒pUDK-HGF的大规模制备和质量分析
    MBL is synthesized by liver cell and secreted into the blood, but the concentration of MBL in blood plasma is very low (~1 mg/L), which makes preparing MBL in large-scale impossible and the scientific research using MBL expensive.
    MBL由肝细胞合成并分泌入血,但人血浆中MBL含量极低(~1mg/L),这使得科研和临床应用MBL不但花费高昂而且不可能大规模制备
    In this paper, the design, experiment and measurement results of ~(153)Gd production by irradiated Eu_2O_3 were described.
    本文介绍了由照射Eu_2O_3大规模制备~(153)Gd的设计、实验和测量结果。
    Conclusions The findings suggested that HRP Ⅱ had been successfully expressed in pEP8c/BL21(DE).
    结论恶性疟原虫HRPⅡ在原核表达系统pET8c/BL21(DE3)中获得成功表达,为基因工程大规模制备生产HRPⅡ抗原奠定基础
    Conclusion This simple method with high yield can be used for laboratory research and large-scale preparation.
    结论本法简单、产率较高,可用于实验室研究和大规模制备
    Conclusion The above findings suggested that tdh ge ne had been successfully expressed i n Trc99A /JM109and paid the preliminary foundation for preparing anti -TDH poly -and /or monoclonal antibod ies used to the diagnosis,con-structing the vaccine candidate and elucidating pathogenesity of Vibrio parahaemolyticus.
    结论tdh基因在原核表达系统Trc99A/JM109中获得成功表达,为基因工程大规模制备TDH抗原,制备抗TDH的多克隆和/或单克隆抗体,构建基因工程菌苗,阐明该菌的致病机制打下了基础。
    Conclusion The results suggested that trh gene was successfully expressed in pGEX - 3X/DE3 and laid the preliminary foundation for preparing anti- trh poly-and/or monodonal antibodies used to the diagnosis, constructing the vaccine candidate and elucidating pathogenecity of Vibrio parahaemdyticus .
    结论:trh基因在原核融合表达系统pGEX-3X/DE3中获得成功表达,为基因工程大规模制备高纯度TRH抗原、构建基因工程菌苗、阐明该菌的致病机制奠定了基础。
    Conclusion TRH gene had been successfully expressed and pure protein was obtained through pGEX 3X/DE3. This paid the preliminary foundation for preparing anti TRH poly/monoclonal antibodies for diagnosis, constructing the vaccine candidate and elucidating pathogenesity of Vibrio parahaemolyticus.
    结论 trh基因在原核融合表达系统pGEX 3X/DE3中获得成功表达 ,并得到纯度较高的TRH蛋白 ,为基因工程大规模制备高纯度TRH抗原、制备抗TRH的多克隆和 (或 )单克隆抗体、构建基因工程菌苗、阐明该菌的致病机制奠定了基础
    Isolated carbon nanotubes with lengths ranging from 200 nm to 600 nm were produced directly with high yield of 15 g/h when alcohol was chosen as carbon source.
    该文以乙醇为碳源,直接大规模制备长度为200~600nm,以单根状态存在的离散碳纳米管,产量为15 g/h。
    Isolated Mn2O3 nanotubes/fibers were prepared at a large scale with liquid-phase catalysis method.
    采用简单的液相催化法实现了完全离散的Mn2O3纳米管/纤维的大规模制备.
    AIM: To prepare pure human bone morphogenetic protein mature peptide rhBMP-4m and rhBMP-2m in large scale.
    目的:大规模制备人骨形成蛋白成熟肽(hBMP-m):hBMP-4m和hBMP-2m.
    Large Scale Preparation of Solubilized Carbon Nanotubes
    可溶性碳纳米管的大规模制备
 

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