• The fusion protein was obtained by purifying protein a.

    蛋白a纯化获得电泳融合蛋白。

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  • ELISA test confirms the specificity of this fusion protein.

    ELISA实验显示重组蛋白抗原特异性良好

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  • Objective: To express and purify the fusion protein of galectin-1.

    目的表达纯化半乳糖凝集- 1融合蛋白

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  • The inhibition ratio of the fusion protein was tested by MTT method.

    MTT检测融合蛋白黑色素瘤细胞的体外抑制

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  • Respiratory Syncytial Virus (RSV), Fusion Protein, Clone: 0681, Mab anti.

    呼吸道合胞病毒RSV),融合蛋白克隆号: 0681,单克隆抗体。

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  • Respiratory Syncytial Virus (RSV), Fusion Protein, Clone: 0631, Mab anti.

    呼吸道合胞病毒(RSV),融合蛋白克隆号:0631,单克隆抗体。

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  • Conclusion The GRA7 gene may be expressed as a GST fusion protein in E. coli.

    结论GRA7基因大肠埃希菌中以gst融合蛋白的形式得到表达

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  • Neuropeptide y; Fusion protein; Inclusion body; Purification; Bioinformatics.

    人神经肽y融合蛋白包涵纯化生物信息学

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  • Monoclonal antibody is produced by immunizing animals with a GST fusion protein.

    单克隆抗体通过合成GST融合蛋白免疫动物制备。

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  • Monoclonal antibody is produced by immunizing animals with a BMP4 fusion protein.

    单克隆抗体BMP4融合蛋白免疫动物产生。

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  • Then, a fusion protein expression system was used to express the TNF half molecule.

    融合蛋白表达系统分子进行大肠杆菌表达

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  • Results: The CAT gene was cloned correctly and it's fusion protein was expressed in E.

    结果:成功克隆CAT基因片段,并大肠杆菌中得到融合蛋白表达

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  • Conclusion Adopting fusion protein P53 (PTD-P53) to treat lung cancer would be available.

    结论采用PTD -P 53治疗肺癌会是一种有效的途径。

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  • The hematopoietic and chemotactic activities of the fusion protein were investigated in vitro.

    研究了融合蛋白在体外促造血细胞增殖活性对免疫细胞的趋化活性。

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  • Results the fusion protein expressed in e. coli account for 20% of the total bacterial protein.

    结果融合蛋白表达菌体总蛋白的20%。

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  • The paper describes process of recombinant fusion protein in purification and existing problems.

    本文论述了基因重组融合蛋白纯化过程存在问题

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

    目的构建凋亡素原核表达系统,以制备抗原物质凋亡素融合蛋白

    youdao

  • The purified fusion protein was used as antigen to immunize rabbit for further gene function study.

    基因的表达成功,功能进一步深入研究奠定了基础。

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  • Cell density cultivation and high level expression of recombinant urease a fusion protein in Helicobacter pylori.

    目的高密度培养重组细菌高效表达重组幽门螺杆菌尿素酶a融合蛋白

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  • The GST-MBD4 fusion protein was purified from cell lysates using glutathione Sepharose 4b affinity chromatography.

    谷胱甘肽琼脂糖凝胶4b亲和介质菌体裂解液中纯化了GST -MBD4融合蛋白

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  • Purpose to study the effect of different factors on the efficiency of cleaving fusion protein with cyanogen bromide.

    目的研究不同因素溴化氰切割融合蛋白影响

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  • Conclusion: PC-1NF fusion protein may inhibit the proliferation, induce apoptosis and decrease ECM production of RMC.

    结论PC - 1nf融合蛋白抑制大鼠系膜细胞增殖诱导细胞凋亡减少细胞外基质合成。

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  • This fusion protein prevents certain blood cells from maturing and leads to an accumulation of immature leukemia cells.

    融合蛋白阻止特定血液细胞分化成熟,使幼稚细胞堆积

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  • The PP65 protein was expressed on the surface of the T7 as head fusion protein. There were 5 to 15 copies on the each phage.

    PP 65目的蛋白融合蛋白形式表达T7噬菌体蛋白部位,每个噬菌体颗粒表面可表达5 ~15个拷贝

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  • Monoclonal antibody is produced by immunizing animals with a fusion protein containing the cytoplasmic domain of human EGF receptor.

    该单克隆抗体通过包含EGF受体胞质融合蛋白免疫动物而制备的。

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  • If the fusion protein of VP1 and VP2 that was expressed in E. coli can form neutralizing antigen epitopes, this problem is resolved.

    如果大肠杆菌表达VP1VP2融合蛋白形成中和抗原表位,则解决了这个问题。

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  • Membrane fusion within the Paramyxoviridae family of viruses is mediated by a surface glycoprotein termed the "f", or fusion protein.

    副粘病毒病毒融合表面糖蛋白F蛋白介导的。

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  • Fusion protein is the main protective antigen of NDV and the primary structure of fusion protein determines the virulence of the virus.

    蛋白不仅NDV主要保护性抗原,而且F蛋白一级结构(氨基酸顺序)决定病毒力。

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  • RESULTS: Fusion protein existed in supernatant of the bacteria lysate and its expression level was about 7% of the total bacteria protein.

    结果融合蛋白以可溶性形式存在细菌裂解上清中,表达量为体总蛋白量的7%。

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  • To investigate the function of PRAK in vivo, a GST fusion protein of PRAK was used as a bait and screened through T7 phage display system.

    为了研究PRAK细胞内确切功能,我们利用GST-PRAK作为诱饵通过T7噬菌体展示系统进行了筛选

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