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采用磁珠细胞分选法进行高梯度磁性细胞分离。

High gradient magnetic cell separation with MACS.

作者信息

Miltenyi S, Müller W, Weichel W, Radbruch A

机构信息

Institute for Genetics, University of Cologne, West Germany.

出版信息

Cytometry. 1990;11(2):231-8. doi: 10.1002/cyto.990110203.

Abstract

A flexible, fast and simple magnetic cell sorting system for separation of large numbers of cells according to specific cell surface markers was developed and tested. Cells stained sequentially with biotinylated antibodies, fluorochrome-conjugated avidin, and superparamagnetic biotinylated-microparticles (about 100 nm diameter) are separated on high gradient magnetic (HGM) columns. Unlabelled cells pass through the column, while labelled cells are retained. The retained cells can be easily eluted. More than 10(9) cells can be processed in about 15 min. Enrichment rates of more than 100-fold and depletion rates of several 1,000-fold can be achieved. The simultaneous tagging of cells with fluorochromes and very small, invisible magnetic beads makes this system an ideal complement to flow cytometry. Light scatter and fluorescent parameters of the cells are not changed by the bound particles. Magnetically separated cells can be analysed by fluorescence microscopy or flow cytometry or sorted by fluorescence-activated cell sorting without further treatment. Magnetic tagging and separation does not affect cell viability and proliferation.

摘要

开发并测试了一种灵活、快速且简单的磁性细胞分选系统,用于根据特定细胞表面标志物分离大量细胞。依次用生物素化抗体、荧光染料偶联抗生物素蛋白和超顺磁性生物素化微粒(直径约100纳米)染色的细胞,在高梯度磁性(HGM)柱上进行分离。未标记的细胞通过柱子,而标记的细胞则被保留。保留的细胞可轻松洗脱。约15分钟内可处理超过10⁹个细胞。可实现超过100倍的富集率和数千倍的去除率。用荧光染料和非常小的、不可见的磁珠同时标记细胞,使该系统成为流式细胞术的理想补充。结合的颗粒不会改变细胞的光散射和荧光参数。磁性分离的细胞无需进一步处理即可通过荧光显微镜或流式细胞术进行分析,或通过荧光激活细胞分选进行分选。磁性标记和分离不影响细胞活力和增殖。

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