1) Confocal laser scanning microscopy
激光共聚焦扫描显微镜
1.
Then these biofilms were visualized by fluorescence stainning with LIVE/DEAD bacterial vitability kit and were observed by confocal laser scanning microscopy (CLSM).
生物膜进行荧光染色,激光共聚焦扫描显微镜(CLSM)观察。
2.
Method Confocal laser scanning microscopy (CLSM) was combined with fluorescencedouble-labelingtechnique to observe the position a nd expression of PTEN.
方法 采用激光共聚焦扫描显微镜光学切片和荧光探针的双重标记技术对三株细胞中PTEN的表达和分布情况进行检测。
3.
Western blot analysis and the confocal laser scanning microscopy(LSCM)were used to further verify the e.
采用比较蛋白质组学方法分离鉴定差异表达蛋白-GBLP,Western blot法和激光共聚焦扫描显微镜(LSCM)分别验证经R/S-PRO作用后,HUVEC细胞中GBLP的表达丰度差异和细胞内定位。
2) Confocal laser scanning microscope
激光共聚焦扫描显微镜
1.
Confocal laser scanning microscope was used to observe its subcellular localization.
方法应用免疫组织化学法测定KIAA0280在大鼠急性脑缺血后在缺血与非缺血区表达的差异,利用激光共聚焦扫描显微镜检测KIAA0280的亚细胞定位。
2.
Immunohistochemistry and double immunofluorescent labeling techniques combined with confocal laser scanning microscope analysis were used to investigate the characteristic spatial induction profile of nestin following a transient middle cerebral artery occlusion in adult rat brain.
应用免疫组化和免疫荧光双标技术结合激光共聚焦扫描显微镜,观察缺血性脑损伤后脑内nestin的表达及其细胞类型。
3.
The development of biofilms in 48 hours in vivo was observed and the vitality and thickness of earlier mature biofilms were measured by confocal laser scanning microscope and the vital fluorescence techniques.
方法建立原位菌斑生物膜模型,运用激光共聚焦扫描显微镜结合荧光染色技术观察原位菌斑生物膜0～48h的发育过程及48h菌斑生物膜的活性和厚度。
3) Laser scanning confocal microscope
激光共聚焦扫描显微镜
1.
Methods Using Fluo-3/Am as fluorescent indicator of Ca 2+ i and it was measured by laser scanning confocal microscope system.
方法以800nmol/LH2O2刺激WB细胞,采用Fluo-3/AM作为荧光指示剂,以激光共聚焦扫描显微镜测定不同条件下犤Ca2+犦i荧光值的改变以反映犤Ca2+犦i含量的变化。
4) Laser confocal scanning microscope
激光共聚焦扫描显微镜
1.
Methods: Cell was cultivated and detected with the flow cytometry and laser confocal scanning microscope methods for the oncogene PTEN expression and location.
01);激光共聚焦扫描显微镜检测PTEN主要表达在细胞核和细胞浆,分布与分化程度有关,细胞核表达强度CNE1
2.
Methods: The changes of Ca 2+ content in ischemic neurocytes were observed by using laser confocal scanning microscope.
方法 :利用激光共聚焦扫描显微镜观察缺血区活体脑片中脑细胞内Ca2 +的变化。
5) confocal laser scanning microscope(CLSM)
激光共聚焦扫描显微镜
1.
Methods Confocal laser scanning microscope(CLSM) and flow cytometry(FCM) were used in this study.
方法 采用激光共聚焦扫描显微镜和流式细胞技术进行观察与检测。
2.
Confocal laser scanning microscope(CLSM) was used in this study 24 hours later;(2) Add double distilled water into t.
(1)空白组加入双蒸水,实验组加入不同浓度Hepcidin(双蒸水配制),干预24h后用激光共聚焦扫描显微镜(CLSM)检测;(2)空白组加入双蒸水,实验组加入不同浓度的DFO和FAC,分别干预后立即用激光共聚焦扫描显微镜检测。
6) laser scanning confocal microscopy
激光扫描共聚焦显微镜
1.
Study of the change of substance P(SP) in the rat cerebellar cortex after hepatocirrhosis by laser scanning confocal microscopy;
肝硬化后大鼠小脑皮质中P物质(SP)的变化及其意义——荧光免疫组化技术结合激光扫描共聚焦显微镜的研究
2.
Free Ca2+ measurement in cultured macrophages of chick embryosby laser scanning confocal microscopy with Fluo-3/AM;
激光扫描共聚焦显微镜和Fluo-3/AM检测细胞内游离钙
3.
The Choices and Applications of Fluorescent Probes in the Laser Scanning Confocal Microscopy;
激光扫描共聚焦显微镜荧光探针的选择和应用
补充资料：扫描电子显微镜(见扫描电子显微术)
扫描电子显微镜(见扫描电子显微术)
scanning eleetron mieroseoPe
扫描电子显微镜scanning eleetron mieroseope见扫描电子显微术。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条