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1)  Immunofluorescence histochemical staining method
免疫荧光组化染色
2)  fluorescent immunohistochemistry
免疫荧光组织化学染色
3)  immunohistofluorescence stain
免疫组织荧光染色
4)  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。
5)  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。
6)  Fluorescent Immunochemistry Stain
荧光免疫染色
补充资料:染色体组型
分子式:
CAS号:

性质:又称染色体组型,一个细胞的特有的染色体构成。与表型相对应。记载一组染色体的长短、粗细、着丝粒的位置的图示。根据生物种类的不同,染色体的数目和形态是各自固定的,故通过核型比较可进行分类学上的亲缘关系推测。由于采用染色体显带法,这样就能作出更为准确的比较。在培养细胞中,由于转化作用,在多数情况下核型会发生变化。此外,与正常组织相比,核型发生变化的细胞能更多地显示出有肿瘤形成的可能。

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