Objective To produce recombinant insect cells by Baculovirus expression vector system.
目的利用杆状病毒表达载体系统制备重组乙型肝炎病毒核心蛋白.
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Objective : To construct inhibin expression vector with high immunogenicity.
目的: 构建高免疫原性的抑制素真核表达载体.
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Objective To construct a prokaryotic expression vector for therapeutic Alzheimer disease ( AD ) vaccine.
目的构建 阿尔采默 病治疗性疫苗原核表达载体.
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Gene sequencing indicated the expression vector pVITRO FSH α? ? - CTP was successfully constructed.
通过基因测序鉴定FSHβ-CTP序列正确.
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The sqHAS gene was ligated into expression vector pSE 380 under trc promoter.
构建表达质粒pSE-sqHAS并转化大肠杆菌DH5α,诱导培养后在细胞膜中检测到sqHAS蛋白及活性.
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RESULTS: The eukaryotic expression vector pIRES 2 - EGFP containing the truncated human AIF ( AIF ? ? 1 - 480 ) gene was successfully constructed.
结果: 成功构建了人截短型AIF ( AIF△1480 ) 基因的真核表达载体.
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Objective To construct eukaryotic expression vector of siRNA specific for ? ? - site APP cleaving enzyme ( BACE ).
目的构建β淀粉样前体蛋白裂解酶 ( BACE ) 特异性小干扰RNA真核表达载体.
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RESULTS: The eukaryotic expression vector containing the truncated human AIF ( AIF ? ? 1 - 400 ) gene was successfully constructed.
结果: 经酶切鉴定与测序证实,带有 AIF △ 1-400 的真核表达载体构建成功.
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Conclusion The baculovirus expression vector pAC - HBs - Fc for complete IgG antibody against HBsAg was successfully constructed.
结论已成功构建表达载体pAC-HBs-Fc,为表达抗人HBsAg的IgG全抗体奠定了基础.
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Conclusions 1 . The expression vector pS 2 - DTA contains the EWS - FLI - 1 binding sequence and the DTA gene sequence.
结论1、我们通过定向克隆的方法,成功地构建了含 EWS -FLI-1特异结合序列和白喉毒素A链基因的真核表达载体.
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The cDNA was subcloned into prokaryotic expression vector pET 3 d and overexpressed in E . coli BL 21 ( DE 3 ).
将该cDNA插入原核表达载体pET3d并在 大肠杆菌 BL21 ( DE3 ) 中过量表达.
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Objective : To construct expression vector of human ID 4 gene promoter on the basis of bioinformatics analysis.
目的: 基于生物信息学分析构建人ID4基因启动子表达载体,以其作为研究ID4基因启动子表达调控分析的工作基础.
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Methods An eukaryotic expression vector encoding Hantaan virus S gene coding region was constructed.
方法利用基因重组技术,构建含汉滩病毒S片段编码区基因的真核表达质粒.
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RESULTS: The eukaryotic expression vector containing the truncated human AIF ( AIF 1 - 400 ) gene was successfully constructed.
结果: 经酶切鉴定与测序证实,带有 AIF1 -400的真核表达载体构建成功.
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For mass production of hEGF, Bombyx mori baculovirus expression vector system was adopted in this experiment.
为了高效表达人表皮生长因子, 我们采用了家蚕杆状病毒表达系统(Bombyxmoribaculovirusexpressionvectorsystem,BMBEVS).
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