位于该调控序列内的ALB高效表达。
The exogenous gene ALB was highly expressed in the regulating sequence.
该突变体可在酵母表达系统实现高效表达。
The mutant may be he efficiency expressed in yeast expression system.
目的构建人il -12的高效表达载体。
Objetive to construct human IL 12 efficient expression vector.
外源基因在该基因工程菌中得到了高效表达。
The gene was highly expressed in the engineering bacterial strain.
结论已成功构建了2cvn融合基因，并获得高效表达。
Conclusion 2cvn fusion gene was successfully constructed and highly expressed.
结果表明，该酶基因在球形芽孢杆菌中获得了稳定、高效表达。
It was showed that the lysostaphin gene could express stably in high level in Bacillus sphaericus.
方法在原核表达系统中高效表达重组人3型腺病毒六邻体蛋白。
Methods Under the optimum expression conditions, the hexon protein of human type 3 adenovirus was efficiently expressed in e.
IPTG诱导突变体在大肠杆菌BL21（DE3）中高效表达。
The mutant was overexpressed in Escherichia coli BL21(DE3) by IPTG induction.
方法：采取目的基因改造及载体构建的方法，以期构建高效表达载体。
Methods: The method of modifying aim gene and constructing vector was adopted to develop a vector with high efficacy.
以EDDIE为融合蛋白是在大肠杆菌中高效表达抗菌肽的一种好方法。
This method provides an excellent way for high expression of antimicrobial peptides when fused with EDDIE.
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。
Cell density cultivation and high level expression of recombinant urease a fusion protein in Helicobacter pylori.
本发明提供了高效表达治疗肿瘤并含有人恒定区全抗体的重组病毒及其用途。
The present invention provides recombinant virus with high efficiency expression to treat tumor and containing all antibody of human constant region.
目的克隆人热休克蛋白70 (HSP70)基因，构建其原核高效表达载体。
Objective to clone human heat shock protein 70 (HSP70) gene for the construction of a prokaryotic expression vector.
目的：构建缺氧诱导表达载体，以介导报告基因在缺氧环境下的特异、高效表达。
Objective: to construct hypoxia-inducible expression vector, which mediated reporter gene to express specially and efficiently in hypoxia environment.
结论建立了两个高效表达突变CD59的真核表达系统，获得阳性克隆细胞株。
Conclusion a eukaryotic system that expressing mutant CD59 cDNA was successfully set up.
结论该方法能方便高效地获得所需的多拷贝基因，为进一步进行高效表达打下基础。
Conclusion With this method the desired multi-copy gene can be obtained that lays the foundation for highly effective expression.
结论：短肽np在大肠杆菌中获得高效表达，为进一步研究其生物活性奠定了基础。
CONCLUSION: Peptide NP could be highly expressed in E. coli. This work builds a solid foundation for further study on its bioactivity.
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。
Conclusion The recombinant expression plasmid constructed by restriction enzyme cleave identification can highly express recombinant human ZP3 protein.
结论：人l -选择素蛋白可在M15大肠杆菌中高效表达，其多克隆抗体效价较高。
Conclusion The recombinant human L-selectin protein can express with high efficiency in E. coli M15. The prepared polyclonal antibody has a high titer.
实现其在CHO - DHFR -细胞中的高效表达，获取生物活性较高的重组蛋白。
AIM: TO obtain high level expression of recombinant human truncated osteoprotegerin (TOPG) with higher bioactivity in CHO-DHFR-cells.
高效表达高比活木聚糖酶是进一步提高木聚糖酶发酵效价、降低其生产成本的有效途径。
High-level expression of xylanase with high specific activity is an effective way to improve xylanase fermentation potency in recombinant host and decrease its production costs.
结论从2周龄大鼠肝组织中成功克隆肝再生增强因子基因，并获得了原核细胞高效表达。
ConclusionThe augementer of liver regeneration gene was cloned from the liver tissue of 2 week old SD rat and the protein encoded by the gene was expressed in the prokaryotic cells.
外源基因在大肠杆菌中高效表达时，通常会形成不溶性、无活性的蛋白聚集体——包涵体。
Over expression of recombinant proteins in Escherichia coli cytoplasm often results in the formation of insoluble inclusion bodies.
高效表达高比活植酸酶是进一步提高植酸酶发酵效价、降低植酸酶生产成本的一个有效途径。
High-level expression of phytase with high specific activity is an effective way to improve phytase fermentation potency and reduce its production cost.
外源淀粉水解酶能在酵母中高效表达并分泌，其主要因素在于：在构建载体时组入强启动子；
The main factors for high efficiency expression and secretion of exogenous amylum hydrolase in S. cerevisiae are as follows: involvement of strong promoter in carrier construction;
另外，还将信息可视化技术应用到情感识别结果的表达上，实现情感信息的生动描述和高效表达。
Furthermore, information visualization technology is also applied in the expression of emotion recognition results to achieve vivid high-level and descriptions of emotion information.
目的：优化重组铜绿假单胞菌外毒素A（PEA）基因工程菌的发酵条件，实现PEA的高效表达。
Objective:To optimize the fermentable conditions of recombinant E. coli BL21 for high level expression of PEA.
表达产物的稳定高效表达及其抗原特异性分析为今后ELISA早期诊断试剂盒的研制提供了依据。
The stable expression of the protein and the analysis of its antigenic specificity provide the foundation for developing the ELISA early stage diagnosis kit.
结论成功克隆人胰腺组织激肽原酶基因，并高效表达融合蛋白，为进一步开发基因工程药物打下基础。
CONCLUSION the fusion protein of the cloned kininogenase gene was highly expressed in E. coli and could be used for the development of its biological products.
获取人蛋白酪氨酸磷酸酯酶4A2（PTP4A2）基因并高效表达纯化，对于产物的体外活性进行测定。
To obtain human protein tyrosine phosphatase type 4A2 (PTP4A2) gene expressed in E. coli and purify the target proteins.
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