克隆与表达弓形虫缓殖子期特异性抗原1（BAG1）的基因，并分析重组抗原的免疫反应性。
Clone and express bradyzoite antigen 1(BAG1) gene of T. gondii, and analyze the immunoreactivity of the recombinant product.
乙酰-D-葡萄糖胺2-差向异构酶基因的克隆及表达。
Cloning and expression of N-acetyl-D-glucosamine2-epimerase.
但是可别指望它拥有一样的个性：它们只不过看上去想像，不过基因表达可能使克隆体令你大失所望。
But don't expect it to have an identical personality: it may look the same but genetic expression may turn it totally mental.
猴hcbp6同源基因的克隆化为研究不同种属来源的HCBP6基因的结构域功能、表达与调控等研究奠定了基础。
The successful cloning of monkey HCBP6 gene paves a way for the study of the relationship of structure and function of HCBP6 genes from different species.
本论文应用基因工程的手段克隆、表达并纯化了人的肝再生增强因子基因。
This dissertation USES the gene engineering method to clone, express and purifies the human ALR gene.
表观遗传修饰在基因表达和克隆胚的早期发育方面有重要作用。
Epigenetic modifications plays an important role in gene expression and the early development of cloned embryo.
建立了筛选质粒表达文库和克隆免疫原基因的技术方法。
We established the techniques of screening the plasmid expression library and cloning the immunogen genes.
木霉纤维素酶基因的克隆与表达研究进展。
The clone and expression of cellulase gene of trichoderma spp.
人血管生成素-1基因的克隆及表达载体的构建，为进一步研究其功能、活性和应用奠定了基础。
The cloning of human angiopoietin 1 gene and construction of it's expression vectors lay a good foundation of further study on the function, biological activity and application.
结论：可通过四环素抗性筛选系统筛选外源基因的高效表达克隆。
Conclussion: We could screen high expressed clone of heterologous gene using tetracycline resistance screening system.
对花粉发育及其特异基因的克隆、表达和调控进行了综述。
The cloning, expression and controlling of specific genes in developing pollen were reviewed briefly.
基因的表达检测证明，克隆菌株具有纤维二糖水解酶活力。
The gene expression test showed that the cloned strains expressed the enzyme activity of cellobiohydrolase.
结论：成功克隆SARS冠状病毒核衣壳蛋白基因全长，并在酿酒酵母中诱导表达成功，有助于抗sars分子疫苗的研究。
Conclusion Successful clone of an integrity SARS-CoV nucleocapsid gene and its effective expression in saccharomyces cerevisiae can be beneficial to the research on SARS vaccine.
在现代分子生物学技术研究中，常常需要对已知位点的侧翼序列进行分析或克隆，以研究基因的遗传表达调控。
In modern research of molecular biology, we usually need to analyse or clone these flanking sequence in given sites, so as to study gene expression and control.
目的构建克隆载体，分析隐匿性乙型肝炎病毒S基因的突变情况，构建其原核融合蛋白表达载体。
Objective To construct the clone vector of S gene in occult hepatitis B virus infection. To analyse its mutations and to construct its prokaryotic expression vector.
结果：成功克隆了CAT的基因片段，并在大肠杆菌中得到其融合蛋白的表达。
Results: The CAT gene was cloned correctly and it's fusion protein was expressed in E.
目的克隆死亡因子相关基因15（MRG15）并研究其在正常晶状体和年龄相关性白内障晶状体上皮细胞中的表达，比较二者的差异。
ObjectiveTo clone the gene of mortality factor related gene 15(MRG15) and to investigate its expression in lens epithelium cell(LEC) of normal and age related cataractous eyes.
结论证实人恶性黑色素瘤a375细胞膜上表达MC 1r蛋白。MC1R基因的成功克隆为其进一步研究提供了必要条件。
Conclusion MC1R protein was successfully expressed on the membrane of human melanoma cell line A375. It provided a basis for the further study on MC1R.
作者介绍了褪黑激素受体1b的结构和功能，褪黑激素受体1b基因的克隆及基因结构、发育性表达与作用、定位与多态性，并讨论了该基因与繁殖季节性的关系。
This review introduced the structure and function of melatonin receptor 1b, the cloning and structure, developmental expression, mapping and polymorphism of melatonin receptor 1b gene.
结论：成功地克隆了人THANK基因，并在大肠杆菌中获得表达，为其功能的研究打下基础。
Conclusion: Human THANK gene was cloned and expressed successfully, which provides a base of further research of THANK gene.
方法：将基因内翻译起始序列合成后克隆到上游含有起始密码和无起始密码的报告质粒中，研究表达水平的差异。
Methods:One of the three internal translation initiation region(TIR) was chemically synthesized and cloned into the report plasmid, and the expression of the report gene was studied.
目前，几种分子生物学技术已用于克隆鉴定多种环境胁迫下的差异表达基因。
Several techniques have been employed to identify the gene whose expression is differentially regulated in response to various environmental stresses in higher plants.
结论：获得的差异表达片段为进一步克隆甲状腺癌相关基因及功能研究奠定了良好的基础。
Conclusions: the differentially expressed fragments establish a favorable foundation for cloning genes related to thyroid carcinoma and continuing with their functional studies.
是最近克隆的脑特异表达的新基因，在大脑发育过程中被选择性地剪接。
Neuronatin (Nnat) is a recently cloned brain - specific gene that is selectively expressed during brain development.
结论原核表达系统可有效克隆较高纯度的CHM - I基因。
Conclusion The more effective CHM-I clone with high purity could be expressed by procaryotic expression system.
目的克隆中国人的肥胖基因，并在大肠杆菌中高效表达人瘦素蛋白。
Objective To clone the obesity gene of Chinese and express human leptin in e.
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。
Objective: To clone and express the gene of human enterokinase light chain which would be used in the cleavage and purification of fusion proteins.
目的克隆、分离血管内皮细胞在致动脉粥样硬化因素作用下差异表达的基因，了解动脉粥样硬化发生的分子机制。
Objective to isolate and clone the differential expressed genes induced by atherogenic factors on vascular endothelium and to understand the molecular mechanism of atherosclerosis.
目的：克隆长双歧杆菌ncc 2705株果糖结合蛋白bl 0033的基因，利用大肠杆菌表达GST -BL 0033融合蛋白并纯化。
Objective: to clone the gene of fructose binding protein BL0033 from Bifidobacterium longum NCC2705, and express and purify fusion protein GST-BL0033 in e.
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.
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