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Histochemical Technique: Densitometry of Nanogram Quantities of Proteins Separated in One-Dimensional Microslab Gels

机译:组织化学技术:在一维微平板凝胶中分离的蛋白质的纳米级数量的光密度法

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摘要

We describe methods for densitometry of electrophoretically separated proteins in 25-millimeter microslab gels. The methods are sufficiently sensitive to use with several individually excised plant cells, for which we describe an extraction procedure. In brief, submicrogram samples are excised from freeze-dried plant tissue. Extraction takes place under oil in microliter droplets of detergent. Proteins are separated by one-dimensional microelectrophoresis (HM Poehling, V Neuhoff 1980 Electrophoresis 1: 90-102) and then stained by a sensitive Coomassie procedure (V Neuhoff, R Stamm, E Hansjorg 1985 Electrophoresis 6: 427-448). The resulting profile is scanned by a computerized densitometer based on the Leitz Diavert MPV Microphotometer. Evaluations and typical data demonstrate the high performance of this system.
机译:我们描述了在25毫米微平板凝胶中电泳分离的蛋白质的光密度测定方法。该方法足够敏感,可以与几个单独切除的植物细胞配合使用,为此我们描述了一种提取程序。简而言之,从冷冻干燥的植物组织中切除亚微克样品。提取在油中以微升洗涤剂滴的形式进行。通过一维微电泳(HM Poehling,V Neuhoff 1980电泳1:90-102)分离蛋白质,然后通过敏感的考马斯方法(V Neuhoff,R Stamm,E Hansjorg 1985 Electrophoresis 6:427-448)进行染色。所得的轮廓通过基于Leitz Diavert MPV显微光度计的计算机密度计进行扫描。评估和典型数据证明了该系统的高性能。

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