fluorescent microscope

Method We observed the expression and location of NFP in the nerve growth cones of primarily cultured chicken embryo spinal ganglion cells by using double immunofluorescent method with fluorescent microscope.

方法采用免疫双荧光染色法，以荧光显微镜观察NFP在初代培养脊神经节细胞生长锥的表达及其定位特征。

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The percentage of TUNEL positive cells was calculated under a fluorescent microscope.

在荧光镜下计数TUNEL阳性细胞的百分数.

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Studies of pollination experiment and the growth of pollen tube under fluorescent microscope on almond

巴旦杏授粉试验及花粉管生长的荧光显微观察

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EM Algorithm and Regularized EM Algorithm for 3-D Images of Fluorescent Microscope

三维荧光显微镜图像的EM和调整EM恢复算法

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Observation of the DiI labeled chondrocytes combined with scaffold by fluorescent microscope

DiI荧光标记的软骨细胞与支架材料复合后的观察

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Analyses of fluorescent microscope observation, PCR and Western blot showed that LIGHT recombinant adenovirus could infect 293 cell lines and replicate in the cells.

荧光显微镜、PCR及Western blot证实，LIGHT重组腺病毒可感染293细胞，并在293细胞内进行有效的复制。

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Laser scanning confocal microscope ( LSCM) was introduced to investigate the 3-D distribution of DNA within the comet and four fluorescent dyes were compared when the single cell gel eletrophoresis was set up.

在建立单细胞凝胶电泳的方法时，对DNA彗星图像进行了共聚焦显微镜观察和三维重建，比较了几种不同荧光染料的染色效果。

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Purpose protein was expressed in this eukaryotic cell and fluorescence could be seen with fluorescent microscope.

获得了目的基因的真核表达，并能观察到荧光。

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DAPI positive cells could be seen at intestinal tissue of MSCs group rats with fluorescent microscope.

治疗组小肠组织荧光显微镜下观察可见DAPI阳性细胞。

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Imaging study of multi-photon ( n ≥ 2) fluorescent confocal microscope

多光子（n≥2）荧光共焦成像特性

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Lucifer yellow CH ( LY) could pass through gap junction to neighboring cells, which were directly observed under inverted fluorescent microscope from different groups and at different hypoxia/ reperfusion by scrape loading and dye transfer ( SLDT).

采用细胞划痕技术，在倒置荧光显微镜下直观地观察不同组别、缺氧再灌注不同时间罗氏黄经过缝隙连接流通情况。

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RESULTS: Expression of RFP gene in HeLa_Y cells was seen under the fluorescent microscope and HeLa_Y cells were screened by FCM.

结果：荧光显微镜下可见红色荧光蛋白在HeLa Y细胞中表达，流式细胞术成功筛选出HeLa Y细胞。

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Vital brain slices were obtained and the calcium fluorescent intensity was examined with laser confocal scanning microscope ( LCSM).

制备活体脑片，检测脑片Ca2+荧光强度，并进行组织病理和电子显微镜检查。

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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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The expression of mbcl-2 a gene was verified by the use of fluorescent microscope and RT-PCR technique.

方法设计一对特异引物,以含mbcl -2 α基因的载体pORF-mbcl-2α为模板,PCR扩增 出mbcl-2α目的片段,克隆至真核表达载体pTracer-EF及 pcDNA3.0中.

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