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用于蛋白质组学分析的IgG和HSA亲和柱再生的快速、简单且有效的技术程序。

Rapid, simple and effective technical procedure for the regeneration of IgG and HSA affinity columns for proteomic analysis.

作者信息

Millioni R, Puricelli L, Iori E, Tessari P

机构信息

Department of Clinical and Experimental Medicine, Chair of Metabolism, University of Padova, Padova, Italy.

出版信息

Amino Acids. 2008 Apr;34(3):507-9. doi: 10.1007/s00726-007-0556-6. Epub 2007 May 21.

Abstract

In plasma and serum, the presence of high-abundance proteins can overwhelm the signals of low-abundance proteins, which then become undetectable either by two-dimensional gels or chromatographic techniques. Therefore, depletion of abundant proteins is a prerequisite to detect low-abundance components. Furthermore, the regeneration of pre-purification tools could be money-saving. We applied an affinity chromatography kit to remove albumin and the immunoglobulin chains from plasma and propose a simple and effective technical procedure for the regeneration of these affinity columns.

摘要

在血浆和血清中,高丰度蛋白质的存在会掩盖低丰度蛋白质的信号,以至于通过二维凝胶电泳或色谱技术都无法检测到低丰度蛋白质。因此,去除丰度高的蛋白质是检测低丰度成分的前提条件。此外,预纯化工具的再生可以节省成本。我们应用了一种亲和色谱试剂盒从血浆中去除白蛋白和免疫球蛋白链,并提出了一种简单有效的这些亲和柱再生技术程序。

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