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1·The labeled cells were observed with laser confocal microscopy.

标记的细胞通过激光共聚焦显微镜观察。

2·Laser confocal microscopy was adopted for observation and photo taking.

激光共聚焦显微镜下观察，拍照。

3·Microglia; 3 D reconstruction; Laser scanning confocal microscopy; Central nervous system.

胶质细胞；三维重建；激光扫描共焦显微镜；中枢神经系统。

4·The uptake and localization of FITC-labeled AODN were detected by laser confocal microscopy.

激光共聚焦显微镜观察FITC标记AODN摄取及细胞内定位。

5·Laser confocal microscopy was employed to reveal the localization of MRP in HEK293 cell line.

利用激光共聚焦显微镜观察MRP在HEK293细胞中的定位。

6·Laser-scanning confocal microscopy was used to monitor the distribution of green fluorescence.

激光共聚焦荧光显微镜观察活细胞内荧光布局。

7·The results showed that it was able to successfully measure cells with the confocal microscopy.

结果表明本方法可成功地应用于共聚焦显微镜测定细胞的研究。

8·Statistically significant correlations were found between clinical data and confocal microscopy data.

临床资料和共聚焦显微镜资料中发现有显著的统计学关联。

9·Laser confocal microscopy was used to observe the locations of Mfn2 gene with and without PKA in cells.

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。

10·Finally, the translocation of fluorescent HBVin living cells was observed by time-lapse confocal microscopy.

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。