• The fusion protein was obtained by purifying protein a.

    蛋白a纯化获得电泳纯融合蛋白。

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  • ELISA test confirms the specificity of this fusion protein.

    ELISA实验显示重组蛋白的抗原特异性良好。

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

    目的:表达和纯化半乳糖凝集素- 1融合蛋白。

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

    MTT法检测融合蛋白对黑色素瘤细胞的体外抑制率。

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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基因在大肠埃希菌中以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;包涵体;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.

    单克隆抗体由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.

    用融合蛋白表达系统对该半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:成功克隆了CAT的基因片段,并在大肠杆菌中得到其融合蛋白的表达。

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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治疗肺癌将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.

    研究了该融合蛋白在体外的促造血细胞增殖活性和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.

    结果融合蛋白的表达量占菌体总蛋白的20%。

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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。

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

    该基因的表达成功,为其功能的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和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.

    用谷胱甘肽琼脂糖凝胶4b亲和介质从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.

    目的研究不同因素对溴化氰切割融合蛋白的影响。

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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融合蛋白能抑制大鼠系膜细胞增殖、诱导细胞凋亡及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.

    这一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目的蛋白以融合蛋白的形式表达在T7噬菌体的头蛋白部位,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.

    该单克隆抗体是通过用包含人EGF受体胞质域的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.

    如果大肠杆菌中表达的VP1和VP2融合蛋白也能形成中和抗原表位,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.

    副粘病毒科病毒的膜融合是由其表面糖蛋白,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.

    蛋白不仅是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于细菌裂解液的上清中,其表达量为菌体总蛋白量的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在细胞内的确切功能,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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  • 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在细胞内的确切功能,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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