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细胞质到细胞核转位的测量。

Measurement of cytoplasmic to nuclear translocation.

作者信息

George Thaddeus C, Morrissey Philip J, Cui Chongwei, Singh Sukhwinder, Bocarsly Patricia Fitzgerald

机构信息

Amnis Corporation, Seattle, Washington.

University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark, New Jersey.

出版信息

Curr Protoc Cytom. 2009 Jan;Chapter 9:9.28.1-9.28.15. doi: 10.1002/0471142956.cy0928s47.

Abstract

A method is described for the quantitative assessment of the translocation of signaling molecules from the cytoplasm to the nucleus in cells. This method utilizes fluorochrome-conjugated antibodies to the signaling molecule and a nuclear dye, and it is based on imagery acquired rapidly in flow with the use of a multispectral imaging cytometer. The analysis correlates the spatial distribution of the stained translocating signaling molecule with nuclear staining, and it generates a quantitative score for each cell using Pearson's correlation coefficient. Examples described in this section use reagents that detect NFkappaB and IRF-7 and measure the translocation of these molecules under stimulating conditions. A protocol for combining cell surface phenotype with cytoplasm to nuclear translocation is also included.

摘要

描述了一种用于定量评估细胞中信号分子从细胞质向细胞核转位的方法。该方法利用与信号分子结合的荧光染料抗体和一种核染料,并且基于使用多光谱成像细胞仪在流动中快速获取的图像。该分析将染色的转位信号分子的空间分布与核染色相关联,并使用皮尔逊相关系数为每个细胞生成一个定量分数。本节所述的示例使用检测NFκB和IRF-7的试剂,并在刺激条件下测量这些分子的转位。还包括将细胞表面表型与细胞质到细胞核转位相结合的方案。

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