• Objective to construct expression plasmid of human motilin receptor.

    目的构建人胃动素受体基因的原核表达载体。

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  • Objective to construct eukaryotic expression plasmid for human insulin-like growth factor 1 (IGF-1).

    目的构建人胰岛素样生长因子1 (IGF - 1)的真核细胞表达质粒。

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  • It was therefore preparation for constructing an expression plasmid vector to express exogenous genes.

    为构建其启动外源基因的质粒表达载体作准备。

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  • After mediated by eukaryotic expression plasmid-liposome, the fused protein was introduced into C2C12 cell system.

    然后经真核表达质粒-脂质体介导,导入C2C 12细胞系。

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  • Objective To clone the human angiotensin-converting enzyme 2 (ACE2)and construct its eukaryotic expression plasmid.

    目的克隆人血管紧张素转换酶2基因(ACE2),并构建其真核表达载体。

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  • The sequence of the cloned SCF is same as the published report. The construction of expression plasmid is identified in a correct way.

    序列分析表明所克隆的SCF序列与文献报道的一致,构建的表达载体经鉴定正确。

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  • Introduction The construction and transfection of eukaryotic expression plasmid are commonly molecular biology method used in medical research.

    序言真核表达质粒的构建和转染是目前医学研究中常用的分子生物学手段。

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  • Objective To construct the prokaryotic expression plasmid expressing woodchuck hepatitis virus core antigen (WHcAg) and prepare polyclonal antibodies.

    目的构建土拨鼠肝炎病毒核心蛋白质粒并进行原核表达、抗体制备。

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  • Conclusion The recombinant expression plasmid constructed by restriction enzyme cleave identification can highly express recombinant human ZP3 protein.

    结论:经酶切鉴定构建的人透明带蛋白3重组表达载体可高效表达重组人zp3蛋白。

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  • The adenoviruses and the eukaryotic expression plasmid have unique practicality in preparing tumor treating medicines and radiotherapy hypersensitivity.

    该腺病毒和真核表达质粒在肿瘤治疗药物、放射治疗增敏的制备中具有独特的实用价值。

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  • Objective to clone the gene activating transcription factor 5 (ATF5), construct the expression plasmid and detect the localization of ATF5 in cultivated cells.

    目的克隆激活转录因子(atf)5,构建其真核表达载体,观察其在细胞中的表达定位。

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  • CONCLUSION: a recombinant eukaryotic expression plasmid of amastin gene of Leishmania Donovani was successfully constructed, and can be expressed stably in the NIH3T3 cells.

    结论:成功地构建杜氏利什曼原虫无鞭毛体蛋白基因的真核表达重组质粒,并且该基因在NIH3T3细胞中获得了稳定表达。

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  • To clone mouse interleukin 4 (mIL-4) truncated gene, construct its eukaryotic expression plasmid pFB-mIL4 and express the truncated protein (murine IL-4 receptor antagonist).

    构建小鼠il -4截短型基因真核表达质粒,表达小鼠il - 4受体拮抗体蛋白。

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  • Conclusions a clone of murine GAD65 is successfully constructed. It is a basis step for further construction of expression plasmid that expresses GAD65 and for immunologic intervention of T1DM.

    结论成功的克隆了小鼠gad65基因,为构建GAD65基因疫苗以及糖尿病的免疫干预治疗打下基础。

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  • Conclusions a clone of murine GAD65 is successfully constructed. It is a basis step for further construction of expression plasmid that expresses GAD65 and for immunologic intervention of T1DM.

    结论成功的克隆了小鼠gad65基因,为构建GAD65基因疫苗以及糖尿病的免疫干预治疗打下基础。

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