目的克隆与原核表达“牵引丝蛋白基因”单体六聚物，为开展具有不同长度系列的“牵引丝蛋白基因”单体多聚物的功能研究奠定基础。
Objective To clone and express the hexamer of the gene of spider dragline silk protein, as a foundation of further research on the functions of the dragline silk protein gene of different lengths.
目的将肌腱蛋白-R不同功能片段在原核中表达、纯化，并研究其初步的生物学功能。
AIM To express and to purify recombinant tenascin R domains and to study their functions.
结论利用原核表达体系成功地表达了不同分子质量的颗粒溶素融合蛋白，为颗粒溶素的后续研究奠定了基础。
Conclusion Different molecular weight granulysin were successfully expressed using prokaryotic expression system, which would be helpful for the further study of granulysin.
本研究成功利用原核表达系统实现了对CT抗原NY-ESO-1的可溶性表达。
So human CT antigen NY-ESO-1 could be successfully expressed in prokaryotic expression system.
实验成功构建了CHIPS蛋白的原核表达系统，为CHIPS免疫原性研究及蛋白的其他功能研究奠定了基础。
The successful construction of the CHIPS protein's prokaryotic expression system in this study has laid a foundation for further study on the protein's immunogenicity and other functions.
结论已成功构建了人hsp70与MAGE - 4抗原表位基因的原核表达载体，为疫苗研究提供了依据。
Conclusion the prokaryotic expression vector for HSP70 and MAGE-4 epitope genes was successfully constructed, which provided a basis for the development of vaccine.
研究目的是分子设计并构建较G-CSF单体分子具有半衰期更长、生物活性更高的新型重组人G-CSF/G-CSF双体分子（简称G-G），并在原核系统进行高效表达。
Molecule design, construction and high level expression in E. coli. of bimolecular G-CSF with longer half life and higher bioactivities than single molecular G-CSF.
尽管研究者已在原核细胞表达系统对胸腺肽的表达进行了研究，但由于原核表达系统缺乏翻译后的加工修饰等缺点，限制了其应用。
Although the thymosin has been successfully expressed in the prokaryotic cell system, its application is restricted because of its deficiency of modification after translation.
结论：原核表达载体的构建、重组蛋白的表达、纯化及多克隆抗体的制备为今后研究该蛋白的功能提供了良好的基础。
CONCLUSION: Recombined prokaryotic expression vector, the purified protein and prepared polyclonal antibody were the necessary materials for further study of this protein.
结论：原核表达载体的构建、重组蛋白的表达、纯化及多克隆抗体的制备为今后研究该蛋白的功能提供了良好的基础。
CONCLUSION: Recombined prokaryotic expression vector, the purified protein and prepared polyclonal antibody were the necessary materials for further study of this protein.
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