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结晶紫染色是比色法(基于双缩脲反应)检测蛋白浓度的可靠替代方法。

Crystal violet staining is a reliable alternative to bicinchoninic acid assay-based normalization.

机构信息

Department of Clinical Pharmacology & Pharmacoepidemiology, Heidelberg University Hospital, Im Neuenheimer Feld 410, Heidelberg, 69120, Germany.

出版信息

Biotechniques. 2022 Sep;73(3):131-135. doi: 10.2144/btn-2022-0064. Epub 2022 Aug 24.

Abstract

Experimental data with cells often require normalization. The frequently used bicinchoninic acid (BCA) assay, in fact, indicates protein content but is influenced by incubation time, pH etc. A simple, rapid and reliable alternative is desirable. Crystal violet stains nucleic acids and proteins and was used to reflect the cell number in 96-well plates. Calibration curves and comparison with BCA confirmed excellent goodness of fit (R: 0.98), conformity (nonsignificant difference of BCA to crystal violet) and reliability of this staining methodology. Crystal violet staining can be used to normalize experimental data to the number of adherent cells present in cell culture plates.

摘要

细胞的实验数据通常需要进行归一化处理。常用的二辛可宁酸(BCA)测定法实际上指示的是蛋白质含量,但会受到孵育时间、pH 值等因素的影响。因此,人们希望有一种简单、快速、可靠的替代方法。结晶紫可染色核酸和蛋白质,用于反映 96 孔板中的细胞数量。校准曲线和与 BCA 的比较证实了该染色方法具有极好的拟合优度(R:0.98)、一致性(BCA 与结晶紫无显著差异)和可靠性。结晶紫染色可用于将实验数据归一化为细胞培养板中存在的贴壁细胞数量。

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