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二维电泳中未染色凝胶的紫外成像密度测定法。

Ultraviolet imaging densitometry of unstained gels for two-dimensional electrophoresis.

作者信息

Yamamoto H, Nakatani M, Shinya K, Kim B H, Kakuno T

机构信息

Shimadzu Corporation, Kyoto, Japan.

出版信息

Anal Biochem. 1990 Nov 15;191(1):58-64. doi: 10.1016/0003-2697(90)90387-o.

Abstract

A system suitable for ultraviolet imaging densitometry of two-dimensional electrophoretic gels that are unstained is described, together with its applications. A flying-spot densitometer linked with a personal computer was used for data acquisition, generation of mapping data, and image processing. Randomly distributed zones of proteins on two-dimensional gels were detected at 280 nm without being stained by two-dimensional scanning, and the densitometric value of each pixel (0.2 x 0.2 mm) was memorized by the computer, which generated a mapping pattern with density contours. The amount and densitometric value of cytochrome c had a linear relationship in the range of 2-200 micrograms. Zone locations of bovine liver proteins separated on two-dimensional gels were indicated on a map expressed in X-Y coordinates, and the pIs and molecular weights could be calculated from the map by use of pI and molecular weight markers on the same gel.

摘要

本文描述了一种适用于二维电泳凝胶紫外线成像光密度测定的系统及其应用,该二维电泳凝胶未染色。使用与个人计算机相连的飞点光密度计进行数据采集、生成映射数据和图像处理。通过二维扫描在280nm处检测二维凝胶上随机分布的蛋白质区域,无需染色,计算机记录每个像素(0.2×0.2mm)的光密度值,并生成带有密度等高线的映射图。细胞色素c的量与光密度值在2-200微克范围内呈线性关系。二维凝胶上分离的牛肝蛋白质的区域位置在以X-Y坐标表示的图谱上显示,并且可以通过使用同一凝胶上的pI和分子量标记从该图谱计算pI和分子量。

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