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1)  Confocal laser scanning microscopy
共聚焦激光扫描显微术
1.
With both two photon laser scanning microscopy and confocal laser scanning microscopy in combination with the fluorescent probe Hoechst 33342, 2′, 7′ dichlorofluorescin diacetate (DCFH DA), Indo 1 and Fluo 3 AM, TCS induced changes in nuclear morphology, reactive oxygen species.
应用双光子及共聚焦激光扫描显微术结合特异性荧光探针Hoechst 3334 2、 2′,7′ 二氯荧光黄双乙酸酯(DCFH DA)、Indo 1和Fluo 3 AM ,首次同时观察了TCS诱导人绒癌细胞 (JAR细胞 )凋亡过程中活性氧自由基 (ROS)和细胞内钙离子浓度 ([Ca2 + ]i)的变化 ,实验结果表明TCS引起的 [Ca2 + ]i 升高和ROS形成参与了TCS诱导的JAR细胞凋亡 ,并且ROS形成和 [Ca2 + ]i 升高有关 。
2)  laser scanning confocal microscopy
激光扫描共聚焦显微术
1.
By using the laser scanning confocal microscopy and plastic (Leica 7022 histeresin embedding kit) semi thin sectioning technique, comparative studies on the fusion of polar nuclei and the formation of the wall of endosperm cells in autotetraploid and diploid rice were carried out.
利用激光扫描共聚焦显微术和塑料包埋半薄切片技术观察同源四倍体水稻极核融合及游离核进一步发育的过程 ,发现同源四倍体水稻约有 1 /3子房极核融合过程和游离核进一步发育与其二倍体原种的基本一致 ;2 /3子房出现各种异常现象 ,如极核未受精、受精异常和胚乳游离核发育滞后等。
2.
Using of the laser scanning confocal microscopy technique and combining the H2O2 fluorescence probe H2DCFDA to exam-ine the production H2O2 in guard cell by exogenous ABA, it showed that the fluorescence intensity in the mutant seedlings was lower than that in wild-type ones.
采用激光扫描共聚焦显微术(LSCM)并结合H2O2荧光探针H2DCFDA检测外源ABA诱导保卫细胞的结果显示,突变体内荧光强度比野生型拟南芥低,暗示此种突变体消除H2O2的能力可能有提高,从而可增强植株抗氧化胁迫的能力。
3)  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 Ca2+ measurement in cultured macrophages of chick embryosby 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
4)  Confocal Scanning Laser Microscope
共聚焦激光扫描显微镜
1.
The γ(austenite)→δ(ferrite) transformation occurring in a duplex stainless steel during heating process was in-situ observed using a confocal scanning laser microscope(CSLM).
利用共聚焦激光扫描显微镜原位观察不同升温速率下双相不锈钢中奥氏体(γ)向高温铁素体(δ)转变的全过程。
2.
Methods The subcellular distribution and accumulation of ADR were studied by confocal scanning laser microscope and flow cytometry.
方法应用共聚焦激光扫描显微镜和流式细胞术研究ADR在细胞内的分布和积聚,以及维拉帕米、BSO、布雷菲尔得菌素、氯喹对细胞内ADR异常分布的影响。
5)  confocal laser scanning microscopy
共聚焦激光扫描显微镜
1.
The Technique of Confocal Laser Scanning Microscopy;
共聚焦激光扫描显微镜技术
2.
Spatial distributions of ammonia oxidizing bacteria(AOB) and nitrobacteria in a renovated suspended carrier biofilm reactor(SCBR) were investigated by using fluorescence in situ hybridization(FISH) with 16S rRNA oligonucleotide probes in combination with confocal laser scanning microscopy(CLSM).
利用16S rRNA寡核苷酸探针荧光原位杂交和共聚焦激光扫描显微镜联用技术,对悬浮载体生物膜内硝化菌群的空间分布规律进行了分析。
3.
The aim of this study is to investigate absorption-promoting mechanism of enhancers and the transport pathway of large hydrophilous molecular across rat nasal epithelium by electron spin resonance(ESR) and confocal laser scanning microscopy(CLSM) technologies.
采用电子自旋共振(ESR)和共聚焦激光扫描显微镜(CLSM)技术研究促渗剂作用机制及促渗剂对亲水性大分子跨鼻黏膜转运途径的影响。
6)  Confocal laser scanning microscope
共聚焦激光扫描显微镜
1.
Objective: To investigate the method of detecting nuclear factor-kappa B (NF-κB) transcriptional activity by using confocal laser scanning microscope (CLSM) combined with fluorescence dual-labeling technique in a rat model of focal cerebral ischemia and reperfusion.
目的:探讨共聚焦激光扫描显微镜(confocal laser scanning microscope,CLSM)结合荧光双标技术检测局灶性脑缺血nuclear factor-kappa B(NF-κB)转录活性的方法。
2.
F-actin marked by FITC-phalloidin and nucleic acid marked by PI in bladder cancer cells were observed by confocal laser scanning microscope to generate the optical sections,then analyzed by image-analysis procedure of confocal laser scanning microscope.
采用共聚焦激光扫描显微镜光学切片技术结合异硫酸氢荧光素 -鬼笔环肽 (FITC- phalloidin)标记纤维肌动蛋白和碘化丙啶 (PI)标记核酸的荧光探针双重标记技术对膀胱癌细胞纤维肌动蛋白进行形态学观察 ,结果可见膀胱癌细胞内纤维肌动蛋白微丝形态完整 ,成细束或细丝状 ,平行排列贯穿于整个细胞或细胞突起 ,在胞质边缘处较密集。
3.
) roots by a GFP_labelled endophytic nitrogen_fixing bacterium, Klebsiella oxytoca SA2, was visualized in a living state with a confocal laser scanning microscope.
)幼苗 ,在接种后 1、2、4、8、12、16和 2 1d ,用共聚焦激光扫描显微镜对水稻鲜根进行光学切片 ,显示了标记菌从水稻根成熟区表面向根内入侵的过程。
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。
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