Suppr超能文献

热介导的高、低分子量蛋白质向硝酸纤维素膜的超快速电泳转移。

Heat-mediated, ultra-rapid electrophoretic transfer of high and low molecular weight proteins to nitrocellulose membranes.

作者信息

Kurien Biji T, Scofield R Hal

机构信息

Arthritis and Immunology Program, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK 73104, USA.

出版信息

J Immunol Methods. 2002 Aug 1;266(1-2):127-33. doi: 10.1016/s0022-1759(02)00103-5.

Abstract

Here, we report an ultra-rapid method for the transfer of high and low molecular weight proteins to nitrocellulose membranes following sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). In this procedure, the electro-transfer was performed with heated (70-75 degrees C) normal transfer buffer from which methanol had been omitted. Complete transfer of high and low molecular weight proteins (a purified protein, molecular weight protein standards and proteins from a human tissue extract) could be carried out in 10 min for a 0.75-mm, 7% SDS-PAGE gel. For 10% and 12.5% gels (0.75 mm), the corresponding time was 15 min. In the case of 1.5-mm gels, a complete transfer could be carried out in 20 min for 7%, 10% and 12.5% gels. The permeability of the gel is increased by heat, such that the proteins trapped in the polyacrylamide gel matrix can be easily transferred to the membrane. When the heat-mediated transfer method was compared with a conventional transfer protocol, under similar conditions, we found that the latter method transferred minimal low molecular weight proteins while retaining most of the high molecular weight proteins in the gel. In summary, this procedure is very rapid, avoids the use of methanol and is particularly useful for the transfer of high molecular weight proteins.

摘要

在此,我们报告一种在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)后将高分子量和低分子量蛋白质转移至硝酸纤维素膜的超快速方法。在此过程中,使用已加热(70 - 75摄氏度)且省略甲醇的常规转移缓冲液进行电转移。对于0.75毫米厚的7% SDS-PAGE凝胶,高分子量和低分子量蛋白质(一种纯化蛋白质、分子量蛋白质标准品以及来自人组织提取物的蛋白质)可在10分钟内完成完全转移。对于10%和12.5%的凝胶(0.75毫米厚),相应时间为15分钟。对于1.5毫米厚的凝胶,7%、10%和12.5%的凝胶在20分钟内可完成完全转移。加热会增加凝胶的通透性,使得被困在聚丙烯酰胺凝胶基质中的蛋白质能够轻松转移至膜上。当在相似条件下将热介导转移方法与传统转移方案进行比较时,我们发现后一种方法转移的低分子量蛋白质极少,而大部分高分子量蛋白质保留在凝胶中。总之,该方法速度非常快,无需使用甲醇,尤其适用于高分子量蛋白质的转移。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验