EGF receptors on the cell membrane were ob-served under a laser scanning confocal microscope after indirect immunofluorescence staining.

The volume of large pollen obtained from the experiment is larger than the normal one.

经染色体加倍处理所获得的2n花粉粒，体积明显比正常的花粉粒大，并将激光扫描共聚焦显微镜用于大花粉粒的倍性鉴定。

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Laser confocal microscopy showed speck dots fluorescence in the PML/ UM-UC-2 nucleus.

激光共聚焦显微镜显示，感染重组PML病毒的膀胱肿瘤细胞胞核内有散在的斑点样的绿色荧光亮点。

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The level of reactive oxygen species ( ROS) was detected with confocal laser scanning microscope and FCM.

ROS水平分别采用激光共聚焦显微镜和FCM检测；

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We observed the change of Ki-67 antigen by laser scanning confocal microscope ( LSCM).

激光共聚焦显微镜观察Ki-67抗原表达量的变化；

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The expression and intracellular localization of EP receptors were determined by RT-PCR and fluorescent immunocytochemistry assay respectively.

采用上述肝癌细胞的细胞涂片或细胞爬片进行荧光免疫细胞化学实验，于荧光显微镜和共聚焦显微镜下观察上述4种EP受体蛋白的表达和定位分布。

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Conclusions CCD fluorescent microscope is superior to laser scanning confocal microscope in collecting the quickly changing fluores-cent image such as DCF.

结论在采集快速变化的荧光图像时，CCD荧光显微镜系统优于激光扫描共聚焦显微镜系统。

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Furthermore, the release of cytochrome c from mitochondria was detected using confocal microscopy in HeLa cells treated with B1.

同时B1作用HeLa细胞后，通过共聚焦显微镜可观察到细胞色素C从线粒体释放。

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Subcellular localization of NMDA receptor protein on neuron membrane by confocal laser scanning microscopy

神经细胞膜NMDA受体蛋白激光共聚焦显微镜亚细胞定位研究

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A newly constructed αⅱ bA2334C GFP fusion protein expressing plasmid was used to determine its subcellular localization by laser confocal scanning microscopy.

为了明确突变亚基的亚细胞定位，构建了αⅡb基因A2334CGFP融合蛋白表达质粒并用激光共聚焦显微镜确定GFP融合蛋白的细胞内定位。

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Changes of auto-fluorescence in H. verticillata leaf under Cd, Cu and Zn stress were analyzed by Laser Scanning Confocal Microscope ( LSCM);

通过激光共聚焦显微镜观察了Cd、Cu、Zn污染后黑藻叶片自发荧光的变化；

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The study reveals that direct naked DNA injection to the muscle shows expression in it, which may bring new treatment for the muscular injury.

而在对侧肢PCR和共聚焦显微镜的结果均为阴性。实验结果表明，肌肉直接注射DNA可以在肌肉得到表达，将会为治疗肌肉损伤带来新的方法。

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The fluorescence intensity was detected with the laser confocal microscope.

3组细胞同时培养48h，用激光共聚焦显微镜观察3组细胞内钙离子的荧光强度。

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Analysis by laser confocal microscopy and flow cytometry revealed that LPS could bind to VEC.

激光共聚焦显微镜和流式细胞仪分析显示LPS能与内皮细胞结合。

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Morphology of the cell division and its content of DNA and RNA were measured under the laser scanning confocal microscope.

本文运用激光扫描共聚焦显微镜和荧光探针技术，检测分裂细胞内DNA、RNA分布和含量的变化。

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Cytochrome c ( Cyt c) release was assessed by confocal laser scanning microscopy.

激光共聚焦显微镜分析细胞色素c（Cytochrome C，CYT C）的释放。

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Discrimination of Anticancer Agent Action Loci at G_2 and M phases by Flow Cytometry and Confocal Microscopic Imaging

流式细胞术联合共聚焦显微镜对G2和M期作用位点的鉴别意义

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The translocation of NF-kB of macrophages was observed by using laser scanning confocal microscopy ( LSCM).

采用激光共聚焦显微镜技术观察巨噬细胞内NF-κB的核移位情况；

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Labeled DCs were detected by confocal microscopy on LN sections or FCM analysis of LN cells. 3.

通过共聚焦显微镜观察或FCM分析，分别检测淋巴结切片、淋巳细胞中的标记DCs。

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Corneal stromal changes under the confocal microscopy after LASIK

共聚焦显微镜下LASIK术后角膜基质的变化

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For the sake of the more accurate assessment system, this paper used the comprehensive evaluation method of Analytic Hierarchy Process and Fuzzy Evaluation. And it gave a detailed description and an example of verification.

为求系统评估结果更为精确，结合超速离心机实际，提出层次分析法与模糊评判法相结合的多层次模糊评判综合评估方法，并进行了详细的介绍和实例验证。

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