激光共聚焦显微镜下观察，拍照。
Laser confocal microscopy was adopted for observation and photo taking.
标记的细胞通过激光共聚焦显微镜观察。
The labeled cells were observed with laser confocal microscopy.
激光共聚焦荧光显微镜观察活细胞内荧光布局。
Laser-scanning confocal microscopy was used to monitor the distribution of green fluorescence.
采用激光共聚焦显微镜观察病毒蛋白在细胞内的定位。
The location of the viral proteins in the cells was observed by laser confocal microscope.
ROS水平分别采用激光共聚焦显微镜和FCM检测；
The level of reactive oxygen species (ROS) was detected with confocal laser scanning microscope and FCM.
方法应用激光共聚焦显微镜结合免疫组织化学双标技术。
Methods: Laser scanning confocal microscope combined with immunohistochemical double labeling methods were used.
应用激光共聚焦显微镜观察DJ - 1在细胞内的定位。
The intracellular distribution of DJ-1 was observed by confocal microscope.
转染2周后，在激光共聚焦显微镜下观察egfp表达情况。
After 2 weeks, the EGFP expression in the rats' retina and choroids were detected by confocal laser scanning microscopy.
诱导表达的菌体在激光共聚焦显微镜下可发射明亮的绿色荧光。
Moreover the induced bacteria could emit bright green fluorescence by confocal laser scanning microscope.
激光共聚焦显微镜检测细胞内游离钙及心肌细胞膜电位的变化。
The changes in the intracellular calcium content and the membrane potential of the myocardial cells were determined by laser confocal microscopy.
使用激光共聚焦仪器能够测量活体细胞内钙离子的浓度和分布。
It can indicate cytoplasm calcium density and distribution using confocal microscope.
诱导表达的菌体在激光共聚焦显微镜下可发射明亮的绿色荧光。
Moreover, the induced bacteria could emit bright green fluorescence by confocal laser scanning microscope.
激光共聚焦显微镜观察到部分ANG与GFAP 共表达现象。
The confocal laser scanning microscope had observed part of coexistence phenomenon of ANG and GFAP.
激光共聚焦显微镜观察FITC标记AODN摄取及细胞内定位。
The uptake and localization of FITC-labeled AODN were detected by laser confocal microscopy.
利用激光共聚焦显微镜观察MRP在HEK293细胞中的定位。
Laser confocal microscopy was employed to reveal the localization of MRP in HEK293 cell line.
最终，应用激光共聚焦显微镜在活细胞中直接观察荧光hbv的转运。
Finally, the translocation of fluorescent HBVin living cells was observed by time-lapse confocal microscopy.
本文目的是探讨耳蜗组织免疫荧光染色及激光共聚焦显微镜技术的应用。
The purpose of this article is to explore The Organization of cochlear immunofluorescent staining and laser scanning confocal microscope technology applications.
激光共聚焦显微镜下观察皮质区、海马ca 1区红色荧光标记细胞数量。
Under the laser confocal microscope, we observed the number of red fluorescence-labeled cells in the cortex and hippocampal CA1 region.
利用激光共聚焦扫描显微镜，分别测定各组肿瘤细胞中的DNA和RNA。
Levels of RNA and DNA in tumor cell membrane in every groups were examined, respectively by laser scanning confocal microtechnic technology.
结论：应用激光共聚焦显微镜技术研究菌斑生物膜结构是一种可行的方法。
CONCLUSION: it was feasible to study the architecture of plaque biofilm by using confocal laser scanning microscope...
方法免疫荧光组织化学双重染色，染色结果在激光共聚焦扫描显微镜下观察。
METHODS Immunofluorescence histochemical double staining technique was used and the staining results were observed with confocal laser scanning microscope.
结果激光共聚焦显微镜观察发现，与RD实验组比较，抑制实验组凋亡细胞明显增多。
Results it was indicated by laser confocal microscopic observations that the number of apoptotic cells in inhibition experiment group was significantly higher than that in RD experiment group.
方法应用免疫荧光组织化学双标记染色技术，在激光共聚焦扫描显微镜下观察染色结果。
Methods Double label immunofluorescence histochemical staining and confocal laser_scanning microscope were used in the experiment.
我们使用激光共聚焦显微镜和扫描电子显微镜，研究了不同扩散条件对所得微胶囊结构的影响。
We then studied the effect of different diffusion conditions on the structure of microcapsules by laser confocal scanning microscope and scanning electron microscope.
并通过流式细胞仪和激光共聚焦显微镜等技术探讨了聚合物在细胞水平的靶向能力及靶向机理。
As revealed by flow cytometry and confocal microscopy, the dendrimer-biotin conjugate exhibits exhibited much higher cellular uptake into cancer cells than the conjugate without biotin.
方法：从牙齿表面获得完整的菌斑生物膜标本，运用激光共聚焦显微镜对其进行断层扫描和分析。
METHODS: the intact dental plaque biofilm specimen was generated on the tooth surface. The specimens of the biofilms were imaged and analyzed by confocal laser scanning microscope.
激光共聚焦显微镜观察完整的和去除蛋白激酶A磷酸化位点的线粒体融合素2基因在细胞中的定位。
Laser confocal microscopy was used to observe the locations of Mfn2 gene with and without PKA in cells.
然后两组分别以神经丝蛋白和神经生长因子受体蛋白免疫荧光双标染色、激光共聚焦显微镜检测移植效果。
Effects of both groups were assayed with neurofilament nf protein and nerve growth factor receptor protein immunofluorescent double labelled staining laser confocal microscopy.
然后两组分别以神经丝蛋白和神经生长因子受体蛋白免疫荧光双标染色、激光共聚焦显微镜检测移植效果。
Effects of both groups were assayed with neurofilament nf protein and nerve growth factor receptor protein immunofluorescent double labelled staining laser confocal microscopy.
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