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通过流式细胞术对产生γ干扰素的细胞进行计数。与荧光显微镜检查的比较。

Enumeration of IFN-gamma-producing cells by flow cytometry. Comparison with fluorescence microscopy.

作者信息

Andersson U, Halldén G, Persson U, Hed J, Möller G, DeLey M

机构信息

Department of Immunology, University of Stockholm, Sweden.

出版信息

J Immunol Methods. 1988 Aug 9;112(1):139-42. doi: 10.1016/0022-1759(88)90044-0.

Abstract

A new intracytoplasmic immunofluorescence staining to detect and quantify human interferon-gamma (IFN-gamma)-producing cells by means of flow cytometry is described. Mononuclear leukocytes, stimulated in vitro to produce IFN-gamma, were fixed and made permeable to antibodies by sequential exposure to paraformaldehyde and the detergent n-octyl-glucoside. Cytoplasmic IFN-gamma was demonstrated by indirect immunofluorescence using IFN-gamma-specific mouse monoclonal antibodies. The staining exhibited a very characteristic morphology and was localized in the Golgi apparatus. An excellent agreement between the enumeration of cytoplasmic IFN-gamma-positive cells by immunofluorescence microscopy and flow cytometry was noted. However, the latter has the advantage of a standardized control, is less labor consuming and is observer independent.

摘要

描述了一种新的胞浆内免疫荧光染色方法,用于通过流式细胞术检测和定量产生人γ干扰素(IFN-γ)的细胞。体外刺激产生IFN-γ的单核白细胞,通过依次暴露于多聚甲醛和去污剂正辛基-β-D-葡萄糖苷进行固定并使抗体可通透进入细胞。使用IFN-γ特异性小鼠单克隆抗体通过间接免疫荧光法显示胞浆内的IFN-γ。该染色呈现出非常典型的形态,定位于高尔基体。通过免疫荧光显微镜和流式细胞术对胞浆内IFN-γ阳性细胞进行计数,结果显示二者具有良好的一致性。然而,流式细胞术具有标准化对照的优势,耗时较少且不受观察者影响。

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