Expressed fusion proteins existed in the form of inclusion body.
重组蛋白以包涵体的形式进行表达。
Expression systems utilizing autolyzing fusion proteins and a novel reducing polypeptide.
NobufusaSerizawa：利用自体裂解融合蛋白质的表达系统及新的还原多。
This invention relates to the detection of among others tumor-specific fusion proteins and protein interactions.
本发明涉及了尤其是肿瘤特异性融合蛋白和蛋白相互作用的检测。
To tackle the above problems, creating fusion proteins with novel insecticidal activities would be an effective way.
构建抗虫融合基因会是一种新的有效的方法用以解决这些问题。
This vector also contains thrombin protease cleavage site to facilitate proteolysis of the bacterial fusion proteins.
为便于从融合蛋白中解离出目的多肽，这个载体中含有特异的蛋白酶裂解位点。
The invention is also directed to the use of at least one of said fusion proteins for the manufacture of a medicament.
本发明还涉及至少一种所述融合蛋白在制备药剂中的用途。
Genetically engineered antibody fusion proteins have more advantages over traditional chemical crosslinking antibody fusion prot...
基因工程抗体融合蛋白比传统的化学交联的抗体融合蛋白具有更多的优越性。
Genetically engineered antibody fusion proteins have more advantages over traditional chemical crosslinking antibody fusion proteins.
基因工程抗体融合蛋白比传统的化学交联的抗体融合蛋白具有更多的优越性。
Aim: to optimize the fermentation conditions of engineering bacteria expressing fusion proteins composed of aprotinin and to purify aprotinin.
目的：优化融合表达抑肽酶基因工程菌的发酵条件，分离纯化抑肽酶。
Objective: To clone and express the gene of human enterokinase light chain which would be used in the cleavage and purification of fusion proteins.
研究目的：克隆表达人肠激酶轻链编码基因，以期应用于融合蛋白的切割与纯化。
To obtain the anti-transferrin receptor scFv and streptavidin(SA) recombinant fusion proteins which were high-efficiently and solubly expressed in E.
拟获得在大肠杆菌中能高效可溶表达的转铁蛋白受体单链抗体与链亲和素（SA）的重组融合蛋白。
Such fusion proteins may be used to improve the nutritional value of plants, such as rice, by enhancing the production of specific essential amino acids in a useable form.
这类融合蛋白可以通过提高可利用形式的特殊必需氨基酸的产量而改进植物，如稻米的营养价值。
Conclusion The recombinant GST-3C protease can be not only applied to the cleavage of fusion proteins, but also be used as a tool-enzyme in TAP system containing 3C recognition sequence.
结论GST-3C蛋白酶不仅可以应用于融合蛋白的酶切，而且为引入3C蛋白酶识别位点的串联亲和纯化（TAP）系统提供又一种酶切工具。
The antigen regions of the aimed gene were selected to be expressed, which could benefit the expression of soluble fusion proteins, and the speciality of serological reaction is satisfied.
结论只表达目的基因的抗原结构域，可以缩短表达片段的长度，有利于获得可溶性目的蛋白，并且具有良好的血清学反应的特异性。
Antibody fusion protein can be particularly used to prepare the immuno directed drug. Genetically engineered antibody fusion proteins have more advantages over traditional chemical crosslink...
基因工程抗体融合蛋白比传统的化学交联的抗体融合蛋白具有更多的优越性。
These results suggest that the existence and changes in their quantity and quality of vesicular nucleating proteins play an important role in vesicle aggregation and fusion.
作者认为，泡中成核效应蛋白的存在或量与质的改变，在泡凝聚与融合过程中起重要作用。
The strategies of fusion protein designing and its advantages and disadvantages in the bioprocessing of recombinant proteins, were introduced in this article.
介绍了构建融合蛋白的策略，优点及其存在的不足。
Using gene fusion technology, polypeptide fusion tags can be engineered into target proteins at the genetic level.
多肽融合标签能够赋予目标蛋白新的特性，便于目标蛋白的定位、追踪、纯化以及结构和相互作用研究。
The SNARE core complex, which forms by the soluble part of SNARE proteins, plays the key part in fusion process.
而由其可溶性部分组成的SNARE核心复合体是发挥融合功能的关键部分。
The portion of the fusion protein accounted for 26% of all the proteins by thin layer gel optical scanning.
薄层凝胶光密度扫描分析结果显示 ，表达的融合蛋白量约占细菌总蛋白的 2 6%。
The portion of the fusion protein accounted for 26% of all the proteins by thin layer gel optical scanning.
薄层凝胶光密度扫描分析结果显示 ，表达的融合蛋白量约占细菌总蛋白的 2 6%。
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