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通过流式细胞荧光测定法定量细胞脱氧核糖核酸。

Quantitation of cellular deoxyribonucleic acid by flow microfluorometry.

作者信息

Coulson P B, Bishop A O, Lenarduzzi R

出版信息

J Histochem Cytochem. 1977 Oct;25(10):1147-53. doi: 10.1177/25.10.72097.

Abstract

This report characterizes for the first time an easy, reproducible means of standardizing the relative fluorescent units normally reported for flow microfluorometry. Absolute values for deoxyribonucleic acid/cell are obtained by using nucleated red blood cells as references. Cell were selected and characterized for the quantitative analysis of deoxyribonucleic acid per cell over a range from 2 pg/cell to 93 pg/cell using literature values for species having nucleated erythrocytes. Fluorescence staining by either acridine-orange (green wavelength) or propidium iodide (red wavelength) gave linear curves over the entire range investigated only when "gain controls" and current are optimized. The range was equivalent to mammalian cell values from 1 N (=3.5 pg deoxyribonucleic acid/cell) to 28 N (=91 pg deoxyribonucleic acid/cell). The standard curves obtained with nonmammalian erythrocytes were compared to mammalian free-cell preparations of bovine thymus and liver cells which fell at 6.8 and 6.9 pg deoxyribonucleic acid/cell, respectively. The routine use of these easily obtainable red blood cells will allow ready comparisons on the basis of absolute values for deoxyribonucleic acid per cell for work between experiments, work between staining procedures and dye types and work between laboratories.

摘要

本报告首次描述了一种简便、可重复的方法,用于标准化通常在流式微量荧光测定中报告的相对荧光单位。通过使用有核红细胞作为参考来获得每个细胞的脱氧核糖核酸的绝对值。使用有核红细胞物种的文献值,选择细胞并对其进行表征,以定量分析每个细胞在2 pg/细胞至93 pg/细胞范围内的脱氧核糖核酸。仅当“增益控制”和电流优化时,吖啶橙(绿色波长)或碘化丙啶(红色波长)的荧光染色在整个研究范围内给出线性曲线。该范围相当于哺乳动物细胞从1N(=3.5 pg脱氧核糖核酸/细胞)到28N(=91 pg脱氧核糖核酸/细胞)的值。将用非哺乳动物红细胞获得的标准曲线与牛胸腺和肝细胞的哺乳动物游离细胞制剂进行比较,后者分别为6.8和6.9 pg脱氧核糖核酸/细胞。常规使用这些容易获得的红细胞将允许在实验之间、染色程序和染料类型之间以及实验室之间的工作中,基于每个细胞脱氧核糖核酸的绝对值进行现成的比较。

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