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。
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。
Results Under fluorescence microscopy, Mycobacterium tuberculosis was stained as golden.
结果在荧光镜下，金胺o荧光染色法将结核杆菌染成金黄色。
The expression of HGF protein was observed by fluorescence microscopy and immunohistochemistry.
用荧光显微镜以及免疫组织化学方法观察HGF表达情况。
The principle of two-photon laser scanning fluorescence microscopy and its applications are reviewed.
文章对双光子激光扫描荧光显微镜的原理及其应用进行了综述。
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。
The system provides improved resolution and contrast, and is well suited for adaptation to fluorescence microscopy techniques.
该系统提供提高了的分辨率和对比度，并还适于匹配荧光显微技术。
Fluorescence microscopy requires an intense light source at the specific wavelengths that excite fluorescent dyes and proteins.
荧光显微镜需要在特定波长的强光源来激发荧光染料和荧光蛋白。
Two-photon fluorescence microscopy (TPM) has now grown up to be an important technique in biology especially neuroscience research.
双光子荧光显微成像技术已逐渐成为生命科学尤其是神经科学研究中的重要技术。
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 tubes were incubated with the breast cancer cells and the extent of attachment to the cell surfaces was investigated by fluorescence microscopy.
管孵育与乳腺癌细胞的程度，重视细胞表面进行了荧光显微镜。
RESULTS: As shown by fluorescence microscopy, the transplanted Scwann cells distributed evenly, and could survive for about 4 weeks after implantation.
结果：荧光显微镜观察显示，异体移植的许旺细胞呈较均匀的散在分布，其存活时间可达4周左右。
The method USES fluorescence microscopy to image individual DNA molecules that have been divided into orderly fragments by so-called restriction enzymes.
该方法应用荧光显微术使单个DNA分子成像，这些单个的DNA分子已经被分成有序的片断，因而被称为限制性内切酶的识别序列。
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。
Fluorescence microscopy showed the particles diameter of SBS in flame retarded SBS modified asphalt reduced which indicated SBS particles were evenly distributed in asphalt.
荧光显微照相表明，进行阻燃处理后sbs的粒径变小，表明在阻燃改性沥青中SBS的分散性更好。
Objective: to compare three sets of fluorescence microscopy imaging systems with each other applied in study of subcellular localization of domestic new photosensitizer HMME.
目的：对三套荧光显微成像系统在国产新型光敏剂HMME亚细胞定位研究中的应用特点及适用范围进行了比较与评价。
With its tremendous potential for understanding cellular biology now poised to become a reality, super-resolution fluorescence microscopy is our choice for Method of the Year.
高分辩率荧光显微镜是我们这一年的年度技术。由于它的巨大潜力，使得人们可以更真实地理解细胞生物学。
Through many years" hard work, we successfully developed the first commercial Laser Confocal Scanning Fluorescence Microscopy and the first Gene- chip Scanner in our country."
通过多年的努力奋斗，成功地开发出国内首台商品化的激光共聚焦扫描荧光显微镜，并且成功开发出国内首台基因芯片扫描仪。
For the first time, we observed the transformation of the J-aggregates morphologies depending on the surrounding humidity by fluorescence microscopy and atomic force microscopy.
利用荧光显微镜和原子力显微镜我们第一次观察到J -聚集体的形貌随着湿度的变化而变化。
Method: Using fluorescence microscopy, electron microscopy, laser scanning confocal microscopy, flow cytometry and DNA gel electrophoresis to demonstrate the presence of apoptosis.
方法：采用荧光显微镜、电子显微镜、激光扫描共聚焦显微镜、流式细胞分光光度计和DNA凝胶电泳等方法和技术观察细胞凋亡。
Increased use of promising methods of diagnosis such as sputum liquefaction and concentration and increased availability of fluorescence microscopy should be explored and encouraged.
应该开发并鼓励增加使用有希望的诊断方法如痰液化和浓缩并增加荧光显微镜术的利用率。
The total internal reflection fluorescence microscopy is one of the most promising bio optical techniques in the world, which has been used to observe single fluorescent molecule directly.
全内反射荧光显微技术是当今世界上最具前途的新型生物光学显微技术之一，可以用来实现对单个荧光分子的直接探测。
To investigate the apoptotic effect in K562 cells exposed to cerium chloride, apoptosis was examined using flow cytometry and apoptosis morphology was detected with fluorescence microscopy.
为了探讨氯化铈对肿瘤细胞凋亡的影响，本实验以K562细胞为研究对象，采用荧光显微镜定性检测细胞凋亡、流式细胞术定量测定细胞凋亡率。
After cultivation, recombinant cells were verified with fluorescence microscopy and sortase activity was detected by fluorescence spectrophotometer from variety of free EGFP's fluorescence intensity.
重组菌经培养，利用荧光显微镜检测重组酵母的荧光强度，然后通过荧光分光光度计检测分选酶与底物相互作用后产生游离的EGFP荧光强度进而确定分选酶的酶活。
The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.
用改良的考马斯亮蓝法对硅片和改性后的硅片进行了蛋白质吸附研究，并采用荧光显微镜观察了胎鼠海马神经细胞在改性前后硅表面的黏附行为。
Objective To explore the conditions under which fluorescence intensity is determined in confocal laser scanning microscopy.
目的对应用激光扫描共聚焦显微镜进行荧光强度的测定条件做了详细的分析。
Methods Immunofluorescence technique was used to investigate whether there was HPK1 in hippocampus neuron under the fluorescence microscope and the confocal microscopy.
方法采用细胞免疫荧光技术通过免疫荧光显微镜和激光共聚焦显微镜观察HPK1是否在大鼠脑细胞中存在；
The research was engaged in the effect of HMC toxin on microfilaments of N and C cytoplasmic male-sterile maize by fluorescence technique and confocal scanning microscopy.
本研究还利用荧光标记和激光共聚焦显微镜相结合的方法，研究了HMC毒素对同核异质体玉米根冠细胞微丝骨架分布的影响。
Single molecule sensitivity is achieved through total internal reflectance fluorescence (TIRF) microscopy, in which a precisely angled laser generates a fast-decaying, evanescent wave.
单分子灵敏度是通过全内反射荧光显微镜(TIRF)实现的，用一个精心设计的激光产生快速衰减的倏逝波。
In most of cases, the laser scanning confocal microscopy images, such as fluorescence stained biomedical nuclei, are blurred and have a wide range of brightness and poor intensity homogeneity.
共焦显微图象如荧光染色细胞核图象，往往是一种比较模糊的图象，并且亮度范围大，灰度均匀度也较差。
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