Hagiwara Makoto, Kobayashi Ken-Ichi, Tadokoro Tadahiro, Yamamoto Yuji
Department of Agricultural Chemistry, Graduate School of Agriculture, Tokyo University of Agriculture, Setagaya-ku, Tokyo 156-8502, Japan.
Anal Biochem. 2009 Jun 15;389(2):171-3. doi: 10.1016/j.ab.2009.03.037. Epub 2009 Mar 28.
Western blot analysis has been a useful method for analysis of expression levels of specific proteins and is conducted after sodium dodecyl sulfate (SDS) or native polyacrylamide gel electrophoresis without staining the gel. However, when it is necessary to analyze the gel, duplicate polyacrylamide gels usually must be prepared, one of which is stained, leading to the consumption of precious sample. Thus, we developed a convenient and efficient Western blotting method using a stained gel. This simple modification should be beneficial for analyzing samples that are limited in quantity and/or samples for which the stained gel serves as the loading control.
蛋白质免疫印迹分析一直是分析特定蛋白质表达水平的一种有用方法,该分析在十二烷基硫酸钠(SDS)或非变性聚丙烯酰胺凝胶电泳后进行,且无需对凝胶进行染色。然而,当需要分析凝胶时,通常必须制备重复的聚丙烯酰胺凝胶,其中一块凝胶进行染色,这会导致消耗珍贵的样品。因此,我们开发了一种使用染色凝胶的便捷高效的蛋白质免疫印迹方法。这种简单的改进对于分析数量有限的样品和/或需要将染色凝胶用作上样对照的样品应该是有益的。