1) immunofluorescence cell staining
免疫荧光细胞染色
1.
METHODS: We used RT-PCR, flow cytometry and immunofluorescence cell staining techniques to observe the expression of PARs on A549 cells.
方法:采用逆转录聚合酶链反应(RT-PCR)、流式细胞仪和免疫荧光细胞染色分析技术分析肺上皮细胞系A549细胞PAR s的表达情况。
2) immunofluorescence staining
免疫荧光染色
1.
Methods Cells were harvested at 0 day,the 3rd day and the 7th day after BGSCs differentiation,then the ratio of Hes-1 positive cells were counted by flow cytometry,and the expression intensity and cell types were detected by laser confocal microscopy after immunofluorescence staining with Hes-1 and GFAP,MAP2 or MBP.
方法对体外培养的人脑胶质瘤干细胞进行诱导分化,于未分化、分化第3、7d收集标本,行Hes-1蛋白免疫荧光染色后流式细胞术检测标本中阳性细胞比例;Hes-1分别与CD133、GFAP、MAP2、MBP蛋白双标免疫荧光染色后,激光共聚焦显微镜下观察Hes-1蛋白表达强度及细胞类型的变化。
2.
The nNOS neurons were detected by immunofluorescence staining.
用免疫荧光染色、RT-PCR和Western blot方法对nNOS神经元数量、nNOS基因和蛋白的表达量进行检测。
3.
The aim of this experiment was to study the effective method of fixation and penetration before immunofluorescence staining in oocytes and early embryos to raise the effect of immunofluorescence staining in them.
本实验旨在探索有效的染色前固定和渗透卵母细胞及早期胚胎的方法,以提高小鼠卵母细胞和早期胚胎免疫荧光染色的效果;同时检测RNA聚合酶Ⅱ(PolⅡ)在小鼠卵母细胞和早期胚胎的表达,探讨PolⅡ在卵母细胞和早期胚胎发育中的作用。
3) Immunofluorescent staining
免疫荧光染色
1.
The purpose of this article is to explore The Organization of cochlear immunofluorescent staining and laser scanning confocal microscope technology applications.
本文目的是探讨耳蜗组织免疫荧光染色及激光共聚焦显微镜技术的应用。
2.
Results Immunofluorescent staining showed predominantly P2X7 and P2X2 receptor expression in OHCs and the distribution of P2X7 receptor overlaped with prestin expression.
结果免疫荧光染色结果:在外毛细胞上仅见P2X2和P2X7两种亚型表达,且P2X7的分布与外毛细胞电运动的基础Prestin蛋白的分布相重合。
4) Fluorescent Immunochemistry Stain
荧光免疫染色
5) Cell immunofluorescence
细胞免疫荧光
6) immunocytofluorescense
免疫细胞荧光
补充资料：免疫学技术荧光激活细胞分类器
[图]
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