期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
干细胞脑内移植有效标记研究:绿色荧光蛋白质粒标记的应用价值 被引量:15
1
作者 关云谦 陈彪 +2 位作者 刘平 邹春林 张愚 《中国临床康复》 CSCD 2004年第13期2506-2508,T002,共4页
目的:观察绿色荧光蛋白(greenfluorescentprotein,GFP)质粒转化小鼠胚胎干细胞(embryonicstemcell,ESC)的效果,以及将转化的胚胎干细胞移植入正常大鼠纹状体后,GFP质粒作为细胞存活情况示踪剂的效果。方法:首先利用感受态大肠杆菌提取... 目的:观察绿色荧光蛋白(greenfluorescentprotein,GFP)质粒转化小鼠胚胎干细胞(embryonicstemcell,ESC)的效果,以及将转化的胚胎干细胞移植入正常大鼠纹状体后,GFP质粒作为细胞存活情况示踪剂的效果。方法:首先利用感受态大肠杆菌提取大量高纯度GFP质粒DNA,然后将GFP质粒与脂质体孵育形成的转化复合物和小鼠胚胎干细胞共同孵育,使GFP质粒转入胚胎干细胞;筛选表达GFP的胚胎干细胞。将筛选后表达GFP的ESC移植入活体大鼠纹状体内,移植21d后,观察表达绿色荧光蛋白的移植细胞的存活情况。结果:GFP质粒转化以后的ES细胞团和单细胞都表达亮绿色的GFP,细胞打散计数证实大约60%的细胞携带GFP,移植21d后,大鼠脑内可见大量表达GFP的移植细胞。结论:脂质体可以将GFP质粒转入鼠的胚胎干细胞,携带有GFP的ES移植后21d,GFP可以作为示踪剂观察移植细胞的存活状况。脂质体辅助的GFP质粒转化胚胎干细胞是移植示踪的较好方法。 展开更多
关键词 干细胞脑内移植 有效标记 绿色荧光蛋白质标记 胚胎干细胞 转基因技术
下载PDF
应用FRAP技术评价蛋白在聚丙烯酰胺-丙烯酸凝胶中的扩散行为
2
作者 崔金磊 周稳稳 +1 位作者 邱玉琴 高云华 《影像科学与光化学》 CAS CSCD 北大核心 2011年第5期336-343,共8页
药物分子从药物载体中的释放行为与载体的结构有密切关系.本实验中采用丙烯酰胺和丙烯酸等材料,运用水相沉淀的方法,制备了4种不同单体配比的聚丙烯酰胺-丙烯酸(P(Am-co-Ac))共聚物水凝胶.运用红外分析方法对P(Am-co-Ac)组成进行表征.... 药物分子从药物载体中的释放行为与载体的结构有密切关系.本实验中采用丙烯酰胺和丙烯酸等材料,运用水相沉淀的方法,制备了4种不同单体配比的聚丙烯酰胺-丙烯酸(P(Am-co-Ac))共聚物水凝胶.运用红外分析方法对P(Am-co-Ac)组成进行表征.使用荧光漂白恢复法(FRAP,fluorescence recovery after photobleaching)观察荧光素FITC标记的牛血清白蛋白(BSA)在聚丙烯酰胺-丙烯酸中的扩散行为,并以激光共聚焦显微镜进行实时成像.实验表明,FITC-BSA在不同单体配比的共聚物中的扩散系数是不同的.通过调节聚合物中单体的配比能够达到控制蛋白释放速率的作用,从而为调控蛋白和多肽类药物的缓控释放提供了可能性. 展开更多
关键词 聚丙烯酰胺-丙烯酸 荧光漂白恢复技术 荧光标记蛋白质 扩散系数
下载PDF
Persistence and Impact of a PGPR on Microbial Communities of Biosolids and Soil Amended with Them
3
作者 L. Fracchia E.B.R. Perotti +2 位作者 A. Pidello M. Rinaldi M.G. Martinotti 《Journal of Environmental Science and Engineering》 2011年第5期578-595,共18页
Survival of the plant-growth promoting rhizobacteria (PGPR) strain Pseudomonasfluorescens 92 in two batches ofbiosolids and soil amended with them and functional and structural shifts occurring in the resident bacte... Survival of the plant-growth promoting rhizobacteria (PGPR) strain Pseudomonasfluorescens 92 in two batches ofbiosolids and soil amended with them and functional and structural shifts occurring in the resident bacterial communities were assessed. Viability of the rifampicin resistant gfp-tagged P. fluorescens 92RTcgfp, inoculated in microcosms consisting of biosolids, soil amended with biosolids and soil, drastically decreased 3-7 days after inoculation in treatments containing biosolids and soil amended with them. The PGPR counts in biosolids were always lower than in soil throughout the experiment whereas, in soil amended with biosolids, were similar or higher depending on the batch of biosolid. Analysis of the community-level physiological profiling (CLPP) revealed a strong impact of the strain on the metabolic activities, as seen in a general uniformity of the inoculated microcosms profiles. According to single-strand conformation polymorphism (SSCP) analysis, the presence of the PGPR had no effect on the resident soil and biosolid eubacterial population, whereas it induced a transient shift in the composition of the resident pseudomonads. In conclusion, biosolids themselves are not suitable as inoculum vehicle for the PGPR nevertheless, their combined incorporation into soil increases the inoculum survival and buffers the competition effects with the resident communities. 展开更多
关键词 Plant-growth promoting rhizobacteria bacterial communities inoculum survival biolog ecoplatestm single-strandconformation polymorphism.
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部