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F-actin was labled and examined using fluorescence microscope. 标记F-actin,荧光显微镜下观察。
Stable expression of AIRE was confirmed by fluorescence microscope, FACS and western blotting analysis. 经荧光显微镜、流式细胞仪及免疫印迹法检测 ,证实 AIRE基因得到了稳定表达。
Construction of Random-Access Scanning Multiphoton Fluorescence Microscope System[J]. 引用该论文吕晓华;占成;张红民;骆清铭;陈伟;曾绍群.
Beginned with basic knowledge of fluorescence,fluorescence microscope characteristics are briefly described. 从荧光的基础知识入手，简略描述荧光星微镜的特点。
Fluord-gold(FG) was injected into C2.Brian sections were made after 1,4 and 8 weeks to observe the survival of rubrospinal neurons under fluorescence microscope. 荧光金(FG)于C2注射,1,4,8周脑切片,荧光显微镜下红核神经元记数观察红核神经元的存活。
Under a fluorescence microscope, the number of fiber stained with Evans blue and dystrophin was counted, analyzed quantitatively with image software. 荧光显微镜下,观察Evans蓝和dystrophin阳性纤维数,图像分析比较。
The permeability ofblood brain barrier (BBB) was evaluated by the dyeing contents of Evans Blue (EB) in hippocampus with fluorescence microscope. 用荧光显微镜观察伊文思蓝(Evans Blue EB)海马区染色程度评估血脑屏障通透性。
Use a total internal reflection fluorescence microscope to observe, the latter can be sent to filter out the background fluorescence. 这里用全内反射荧光显微镜来进行观察，就可以把后者发出的背景荧光过滤掉。
This article introduces the basic principle, instrument, analysis and calculative method on how to take count of bacteria by fluorescence microscope. 介绍了细菌荧光显微镜直接计数法的基本原理、仪器设备、分析和计算方法,并对水样过滤操作方法作了一些改进。
After iDCs were transfected by Adv-CD40L-IRES2-CTLA4Ig, the fluorescence microscope was used to observe the expression of CD40L and CTLA4Ig in iDCs. 2. 腺病毒介导CD40L-IRES2-CTLA4Ig基因转染iDC，荧光显微镜下观察CD40L和CTLA4-Ig在树突状细胞的表达情况；
White and soft callulas were obtained.They are fitful to be observed under fluorescence microscope, having no interference of chloroplast. 优化了愈伤组织的培养条件，得到了质地疏松柔软的白色愈伤，不受叶绿体的荧光干扰，便于进行荧光观察。
After MGC803 cells were exposed to DATS,the typical apoptotic morphological changes were observed under the light microscope and the fluorescence microscope. 在光学显微镜及荧光显微镜下,通过DATS作用后的胃癌细胞出现了凋亡的典型形态学改变;
Hippocampal neuron survival was assessed by MTT method and hippocampal neuron mitochondrial membrance potential (MMP) was evaluated by fluorescence microscope and flow cytometry. 采用荧光显微镜及流式细胞仪观察和检测海马神经元的线粒体膜电位变化。
Result After MGC803 cells were exposed to DATS,the typical apoptotic morphological changes were observed under the light microscope and the fluorescence microscope. 结果在光学显微镜及荧光显微镜下,通过DATS作用后的胃癌细胞出现了凋亡的典型形态学改变;
BDP-PLGA nano-capsules co-loaded with BDP andfluorescein sodium were nebulised to guinea pigs, tissue section of lung were prepared to observe pulmonary distribution with fluorescence microscope. 豚鼠雾化吸入包有荧光素钠的BDP-PLGA纳米囊,取肺组织切片,荧光显微镜下观察肺内分布。
To observe the change of brain tissue and ultrastructure by fluorescence microscope with Evans Blue (EB) dyeing, electro-microscope with La footprint and transmission electro-microscope. 采用荧光显微镜伊文氏蓝(EB)、电镜镧示踪法以及透射电镜观察脑组织的超微结构变化。
The positive cell clones had been obtained after selected by G418. The stable transfection and expression of AIRE in HeLa cells were determined by the fluorescence microscope, FACS and Western blotting. 继续培养 4周 ,用荧光显微镜观察、流式细胞仪 ( FACS)检测和免疫印迹法检测 AIRE基因在 He La细胞中的稳定表达情况。
The subcellular localization was analyzed by fluorescence microscope and confocal. The fluorescence of PF40-GFP fusion protein was detected mainly in the ER, demonstrating that PF40 was mainly localized in the ER. 用荧光显微镜观察,发现PF40的亚细胞定位是在围绕核的内质网以及胞质网格状内质网上。
The BDP-PLGA nano-microcapsules co-loaded with BDP and fluorescein sodium were nebulised to guinea pigs,and their tissue section of lung were prepared to observe the pulmonary distribution of BDP nano-microcapsules with fluorescence microscope. 豚鼠雾化吸入3H-BDP-PLGA纳米微囊,取肺组织切片,荧光显微镜下观察肺内分布。
Results Under the fluorescence microscope, dual immunofluorescent labeling for ZNT3 and Zinc was observed with abundant labeling for both staining in mouse mossy fibers of hippocampus in mice. 结果在小鼠海马苔藓纤维,锌离子和ZNT3蛋白被各自标记,荧光反应阳性。而合并后的图片表明,两者实现完全共区域化。