confocal microscopy

Method: We used confocal microscopy observed the expression of the thrombocytic immune related antigen CD42a, TSP and CD9 on high metastasis lung cancer cell line PG and low metastasis lung cancer cell line PAa.

方法：利用激光共聚焦显微镜观察高转移人巨细胞肺癌细胞PG利低转移人肺腺癌细胞PAa表达的血小板免疫相关抗原CD42a、TSP、CD9的表达情况；

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Confocal microscopy was used to investigate corneal thickness, epithelial and stromal cellular density, and plexus morphology.

用共聚焦显微镜来研究角膜的厚度, 上皮细胞和间质细胞的密度以及基质浅丛的形态.

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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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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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Objective To evaluate the value of confocal microscopy in the diagnosis and examination of early stage keratoconus.

目的了解早期圆锥角膜共焦显微镜的影像特征，评价共焦显微镜（confocal microscopy）对早期圆锥角膜（keratoconus）的临床检查意义和诊断价值。

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Thrombi were imaged via high-resolution confocal microscopy.

血栓的影像通过 高分辨率 显微镜.

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The adhesive strengths of ECs on the PET surfaces were compared under flow condition ( 8^ 19 dyne/ cm+ 2 for 4h), and the expression of F-actin and talin were detected by laser confocal microscopy to study the shear-resistant mechanism of adherent cells.

本研究在体外流动条件下观察结合RGD肽或纤维粘连蛋白的聚酯材料表面粘附内皮细胞的抗剪切能力，并通过观察肌动蛋白和踝蛋白的表达初步探讨影响细胞粘附稳定性的机制。

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The localization of Cx43 proteins were performed by indirect immunofluorescence histochemical analysis and detected by confocal microscopy.

采用间接免疫荧光细胞化学法和激光共聚焦显微镜进行连接蛋白Cx43定位的测定；

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Consequence: we saw that the CD 42 a , TSP and CD 9 expression adqulis on cell surface by confocal microscopy.

结果: 利用激光扫描可见CD9、CD42a、TSP均匀的表达了细胞表面.

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Bright green fluorescence is visualized by fluorescence and confocal microscopy.

在荧光显微镜和激光共聚焦显微镜下观察到强烈绿色荧光。

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Corneal Morphology of Early Stage Keratoconus by Confocal Microscopy in Vivo

早期圆锥角膜共焦显微镜形态学研究

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The application of laser scanning confocal microscopy in the research was the most striking innovation.

试验中激光共聚焦显微技术的应用是此试验的最大创新点。

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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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Confocal microscopy confirmed the internalization of the drug conjugates into the tumor cells.

共聚焦显微镜证实,共轭的药物通过内摄作用进入肿瘤细胞.

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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.

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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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The expression of F-actin and alpha-actinin were analyzed by immunofluorescence and Leica laser scan confocal microscopy.

细胞免疫荧光法和激光共聚焦显微镜观察和测定细胞骨架分子F-肌动蛋白（actin）、α-辅肌动蛋白（actinin）的表达。

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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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Research on High-Precision Acquisitive Method of Surface Coordinate Information Based on Parallel Confocal Microscopy

并行共焦显微探测高精度表面坐标信息获取方法

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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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As a new noninvasive microscopy , confocal microscopy has been used to investigate corneal dystropies.

共焦显微镜作为一种新型的、无创伤的光学显微镜, 已应用于角膜营养不良的研究.

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Observation of the cell division with the confocal microscopy

分裂细胞的共聚焦显微镜观察

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Cultured cardiocyte were loaded with CFDA/ AM fluorescence probes, and the changes of cell& cell communication were examined by laser scanning confocal microscopy.

用CFDA/AM荧光探针负载离体培养的大鼠心肌细胞，在激光扫描共聚焦显微镜下观察细胞内胞间通讯的变化。

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Whether NO and H_2O_2 were concerned with the adjustment in indirect ways was further explored by pharmaceutical experiment and laser-scanning confocal microscopy.

借助药理学试验和激光扫描共聚焦显微镜技术，进一步对该间接效应过程中是否有NO和H2O2的参与进行了探讨。

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Confocal microscopy is an important measurement technique for micro structure.

共焦显微术是一种重要的微小物体测量技术.

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With confocal microscopy on whole cells, our results showed that mitotic phosphorylation of H3 initiated in discrete foci near the nuclear envelope in early prophase cells. Following initiation, H3 phosphorylation appeared to spread throughout the condensing chromatin and reached maximum in early metaphase cells.

共聚焦显微结果显示：H3磷酸化在早前期细胞核膜附近以斑点状起始，之后扩展到整个凝集的染色质上，然后在早中期达到最高水平。

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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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METHODS: The techniques used in this study were brain slice patch clamping whole cell recording, lucifer yellow ( LY) staining, immunofluorescence and laser scanning confocal microscopy ( LSCM).

方法：采用脑片膜片钳全细胞记录、细胞内荧光黄染色、免疫荧光和激光共聚焦显微镜相结合的技术。

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Clinical application of in vivo confocal microscopy through focusing in LASEK and PRK

LASEK与PRK术后角膜组织结构的活体激光共聚焦显微镜观察

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