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High Throughput Absolute Determination of the Content of a Selected Protein at Tissue Levels Using Quantitative Dot Blot Analysis (QDB)

机译:使用定量斑点印迹分析(QDB)在组织水平上高通量绝对测定所选蛋白质的含量

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摘要

Lacking a convenient, quantitative, high throughput immunoblot method for absolute determination of the content of a specific protein at cellular and tissue level significantly hampers the progress in proteomic research. Results derived from currently available immunoblot techniques are also relative, preventing any efforts to combine independent studies with a large-scale analysis of protein samples. In this study, we demonstrate the process of quantitative dot blot analysis (QDB) to achieve absolute quantification in a high throughput format. Using a commercially available protein standard, we are able to determine the absolute content of capping actin protein, gelsolin-like (CAPG) in protein samples prepared from three different mouse tissues (kidney, spleen, and prostate) together with a detailed explanation of the experimental details. We propose the QDB analysis as a convenient, quantitative, high throughput immunoblot method of absolute quantification of individual proteins at the cellular and tissue level. This method will substantially aid biomarker validation and pathway verification in various areas of biological and biomedical research.
机译:缺乏在细胞和组织水平上绝对确定特定蛋白质含量的便捷,定量,高通量免疫印迹方法,这严重阻碍了蛋白质组学研究的进展。从当前可用的免疫印迹技术获得的结果也是相对的,从而阻止了将独立研究与蛋白质样品的大规模分析相结合的任何努力。在这项研究中,我们演示了定量斑点印迹分析(QDB)的过程,以实现高通量格式的绝对定量。使用市售的蛋白质标准品,我们能够确定由三种不同的小鼠组织(肾脏,脾脏和前列腺)制备的蛋白质样品中加盖的肌动蛋白,凝溶胶蛋白样(CAPG)的绝对含量,以及对实验细节。我们建议将QDB分析作为一种便捷,定量,高通量的免疫印迹方法,在细胞和组织水平上对单个蛋白质进行绝对定量。该方法将在生物学和生物医学研究的各个领域中大大有助于生物标志物的验证和途径验证。

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