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通过在蒸馏水中冷冻使细胞裂解后,在96孔组织培养板中使用Hoechst 33258进行DNA荧光测定。

DNA fluorometric assay in 96-well tissue culture plates using Hoechst 33258 after cell lysis by freezing in distilled water.

作者信息

Rago R, Mitchen J, Wilding G

机构信息

Department of Human Oncology, University of Wisconsin Clinical Cancer Center, Madison 53972.

出版信息

Anal Biochem. 1990 Nov 15;191(1):31-4. doi: 10.1016/0003-2697(90)90382-j.

Abstract

A simple assay is described using bisbenzimidazole (Hoechst 33258) to determine cellular DNA content in 96-well tissue cultures plates. At time points of interest, the plates are emptied of media and stored frozen. When the assay is to be performed, cultures are briefly incubated in distilled water and frozen again. This process lyses the cells and allows rapid and thorough mixing of the fluorochrome and cellular DNA. Freezing permits convenient storage of cultures until the time of assay. Experiments can be batched, further reducing processing time and giving better intra- and interexperimental standardization. The assay generates a linear standard curve for DNA fluorescence versus cell number, the range of which is appropriate for microculture wells. This enables the rapid and accurate measurement of cell number involving minimal processing time, making this assay well suited for cell proliferation studies.

摘要

本文描述了一种使用双苯并咪唑(Hoechst 33258)来测定96孔组织培养板中细胞DNA含量的简单检测方法。在感兴趣的时间点,倒掉培养板中的培养基并冷冻保存。进行检测时,将培养物在蒸馏水中短暂孵育后再次冷冻。此过程会裂解细胞,并使荧光染料与细胞DNA快速充分混合。冷冻便于在检测前方便地保存培养物。实验可以分批进行,进一步减少处理时间,并实现更好的实验内和实验间标准化。该检测方法生成了DNA荧光与细胞数量的线性标准曲线,其范围适用于微孔培养。这使得能够在最短的处理时间内快速准确地测量细胞数量,因此该检测方法非常适合细胞增殖研究。

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