With the cell in place, the researchers gradually increased the power of the blue laser and watched how the green fluorescence changed as a result.
细胞放到位置以后，研究者一步步提高蓝色激光的功率，观察绿色荧光的变化。
Endothelial cell attached to synthetic microfibers, stained with microtubules, F-actin and nuclei (2500x), Fluorescence, confocal.
附着在合成超细纤维上的内皮细胞，微管、肌动蛋白和胞核已染色(2500倍)，荧光和激光共焦显微镜。
Methods Fluorescence staining and confocal microscopy were used to study the distribution of contractile proteins in LAM cell.
方法用荧光抗体染色法和激光共焦显微镜观察收缩蛋白在L AM细胞的分布。
Methods Cell culture, immunohistochemistry, nucleus fluorescence labeling, fluorescence retrograde labeling and enzymatic histochemistry technique were used.
方法应用细胞培养、疫组织化学、荧光标记、光逆行追踪和酶组织化学等技术。
The fluorescence indicates the amount of mechanical stress in the host protein and this can be imaged in different parts of a cell or an organism.
荧光显示的是宿主蛋白的机械应力，这可以显示细胞或机体的不同部位的影像。
Blood ingredients were determined by the blood cell analyzer, and erythrocyte membrane fluidity and microviscosity were measured by fluorescence polarization techniques.
利用血细胞分析仪进行血液成分测定，采用荧光偏振法测定红细胞膜流动性和微黏度。
Blood ingredients were determined by a blood cell analyzer, and erythrocyte membrane fluidity and microviscosity were measured by fluorescence polarization technique.
利用血细胞分析仪进行血液成分测定，采用荧光偏振法测定红细胞膜流动性和微黏度。
Formation of single endosomes on cell membrane was analysised by total internal reflection fluorescence microscopy at first.
这是首次用全内反射荧光显微术测定了细胞中的内吞转铁蛋白形成内涵体的过程。
Using the computer multimedia technology and fluorescence microscope, we established the pathology organization analysis and the living cell fluorescence trace system.
采用电脑多媒体技术配合荧光显微镜，建立了病理组织分析及活细胞荧光示踪系统。
Positive cell labeled red fluorescence.
阳性细胞标记为红色荧光。
The expression of cell surface-bound DR4 and DR5 were determined by indirect fluorescence staining and flow cytometry analysis.
用间接免疫荧光染色结合流式细胞技术检测细胞表面DR4和DR5分子表达；
Monochromator is a very important part in living cell fluorescence microscopy system.
单色激发光源是单细胞荧光显微系统中的重要组成部分。
To study the application of capillary electrophoresis and Laser-induced fluorescence in single-protoplast analysis in order to analyze amino acids in wheat embryonal cell.
研究毛细管电泳单细胞分析技术和激光诱导荧光检测技术在植物细胞单细胞分析中的应用，实现单个小麦胚性细胞内氨基酸的分析。
Methods Cell culture, immunohistochemistry, nucleus fluorescence labeling, fluorescence retrograde labeling and enzymatic histochemistry technique were used.
方法应用细胞培养、免疫组织化学、核荧光标记、荧光逆行追踪和酶组织化学等技术。
Four color fluorescence activated cell sorting (FACS) analysis was applied to detect the expression profiles of adhesion molecules and chemokine receptor CXCR 4 on CD34 bright cells.
应用四色荧光活化流式细胞术(FACS)检测CD 34 +细胞其粘附分子及趋化因子受体CXCR -4的表达谱。
Monochromator is very important part in living cell fluorescence microscopy system.
单色激发光源是单细胞荧光显微系统中的重要组成部分。
The experimental results indicated that the fluorescence and RSS of plasma increased with concentration, but the spectra of whole blood and red blood cell first rose and then dropped.
红细胞和全血溶液则同时表现为先升高后降低，并且荧光光谱还出现了蓝移的现象。
When the receptor was activated and had retreated into the cell, the fluorescence dimmed.
当激活受体返回细胞内时，荧光变暗。
Dot plot image of DNA fluorescence could form region of diploid and tetraploid in integrated cell.
结果显示：结构完整的细胞DNA的荧光点图形成二倍体、四倍体的区域。
Objective To investigate the fluorescence quantitative polymerase chain reaction (FQ-PCR) in the giant cell viral hepatitis in value.
目的探讨荧光定量聚合酶链反应(FQ - PCR)在巨细胞病毒性肝炎中的应用价值。
Immunohistochemistry showed that 5f11 located in cell membrane and cytoplasm and fluorescence microscopy proved that DOX located inside the cells.
免疫组化检测发现5f 11定位于细胞膜与胞浆中，而荧光镜检发现DOX分布于细胞内。
The formation of the aleuronic layer cell wall in autotetraploid and its original diploid rice was studied by using the technique of fluorescence microscopy.
利用荧光显微术观察，发现同源四倍体水稻与其二倍体原种的糊粉层细胞壁纤维素物质都存在一个“充实”的过程。
The structure characteristics of aberrant cell, identification marking, fluorescence labeling technologies and methods of cell labeling by fluorescent probe are recommended.
介绍了变异细胞的结构特征、细胞识别与荧光标记技术以及荧光染料探针分子标记细胞的方式。
It was observed by fluorescence microscope that plasmid DNA could be delivered into C2C12 cell lines, and the genes were effectively expressed in receptor cells.
通过在荧光显微镜下的观测，证明质粒dna可被导入C2C 12细胞，并且其所携带的基因可在受体细胞中有效的表达。
METHODS The percentage of androgen receptor positive cells were detected by fluorescence activated cell sorter (FACS).
方法应用荧光激活细胞分离器（FACS）检测雄激素受体阳性的细胞。
Flow cyto fluorescence can be used to obtain the curves of cell numbers vs cellular content, and to explore the relation of cellular DNA content with prognosis in human malignancy.
利用流动细胞荧光测量技术可以获得细胞数量和D N A 相对含量关系曲线，探索细胞D N A 含量和人类肿瘤预测之间的关系。
METHOD The fluorescence simple clone stream mode cell meter was used.
方法采用荧光标记单克隆抗体流式细胞仪测定。
Quantum dots(QD)are fluorescence labels, whose research fields involve biomedical imaging, disease diagnosis, and cell biology.
量子点（QD）是一种荧光标记物，其研究领域涉及生物医学成像、疾病诊断和细胞生物学。
Organelle-cell fluorescence intensity ratio analysis was adopted to study the intracellular distribution of HMME.
采用细胞器-细胞荧光强度比值法，对HMME进行单细胞内分布的定性与定量研究。
Objective To develop a method for acquisition of efficient and stable retroviral packaging cells on the basis of fluorescence-activated cell sorting (FACS) technique.
目的探讨利用荧光激活细胞分选技术获得有效重组逆转录病毒包装细胞系的方法。
应用推荐