| 1. | Statistical study on the law of gene fusion
基因融合规律的统计研究 |
| 2. | Two expression systems were used , one of which was qiaexpress system , the other glutathione s - transferase ( gst ) gene fusion system
)系统和谷胱甘肽s ?转移酶( gst )基因融合表达系统。 |
| 3. | It was confirmed by restriction enzyme digestion analysis that egfp fusion expression plasmids of scfvs were successfully constructed
的序列正确，经酶切鉴定证实成功地构建了绿色荧光蛋白基因融合表达载体。 |
| 4. | The ha 122 protein , when fused to gfp was observed in the nuclei of h . armigera cells , but only in conjunction with wild type hasnpv infection
将ha122与绿色荧光蛋白( gfp )基因融合，在昆虫细胞中瞬时表达。当有病毒感染同时发生时， gfp信号定位在核内。 |
| 5. | The principles , operation and applications of site - directed mutagenesis , gene fusion technology , and post - translational modification methods were introduced emphatically
着重阐述了基因定点突变技术、基因融合技术和翻译修饰技术等新兴定点固定化技术的原理、特点和操作。 |
| 6. | Zhonghua 11 ) at different growth phases . so , the promoter region ofosdd2 gene was cloned and fused with a gus gene , in order to speculate the osdd2 expressing patterns
鉴于基因表达模式不清，克隆了osdd2基因约2kb左右的启动子序列并与gus基因融合，构建植物转化载体。 |
| 7. | The two cdna fragments , ap - 2a full length cdna and ap - 2 a cdna fragments were inserted in frame into gst gene fusion system . with an ap - 2a monoclonal antibody we detected the expression of gst - ap - 2a
将这两段筛选所得cdna片段和ap - 2 cdna全长及ap - 2 cdna的分段形式用gst基因融合系统进行表达，并用ap - 2的单克隆抗体检测了gst - ap - 2融合蛋白表达的情况。 |
| 8. | Based on the foundation research of the interaction of virus and host actin , we recombine gfp gene - a reporter gene - with 5c actin gene of drosophila melanogaster , a gfp - actin fusion gene was obtained
本文在总结前人关于病毒与宿主肌动蛋白相互作用的研究的基础上，利用绿色荧光蛋白基因为标记基因，与果蝇肌动蛋白基因5cactin基因融合，构成gfp - actin融合基因。 |
| 9. | Dna band is about 600 bp when p1asmid was digested by sacii and saci enzyme , and is equal to that of hbsag gene ; but it is about 700bp when plasmid was digested by xhoi and saci enzyme , and is equa1 to the weight of s , . / hbsag fusion gene
经sacll和saclk切电泳可见约600hp的dna带，与hbsag基因大小相当；用xhol和sacl切电泳可见约700hp的dna带，同s …与hbsag基因融合片段的大小相等说明s ； 。 |
| 10. | Northern blot analysis showed the pf40 gene was expressed in all tissue of plant but predominantly in very young tissue such as hypocotyl and bud , the result was further tested by fusion pf40 with gus gene . used different hormone to induce the pf40 gene showed it was regulated by 6 - ba and ga
用pf40基因与gus基因融合表达的结果与northern杂交结果相近， pf40基因主要在植物生长旺盛部位表达。激素诱导实验发现pf40基因是受6 - ba与ga的调控的。 |
