智能洗涤:免疫印迹加速膜洗涤方法。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-04-17 DOI:10.1002/elps.8104
Ethan P Stevenson, Christopher K Schroeder, Richard Chan, Herbert M Geller, Yasuhiro Katagiri
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引用次数: 0

摘要

免疫印迹,也被称为免疫印迹,是生命科学中一个成熟的程序。它通常用于确定特定蛋白质的相对大小和丰度,以及蛋白质的翻译后修饰。虽然这种方法因其简单而被广泛采用,但它可能需要数小时甚至数天才能完成。尽管在减少整个过程时间(特别是抗体孵育)方面做出了相当大的努力,但自免疫印迹技术发展以来,涉及膜冲洗的步骤一直保持不变。在这种情况下,我们推出了一种名为“智能洗涤”的创新设备,通过使用电动沙拉旋转器,可以显着缩短洗涤间隔。智能洗涤的原理类似于家用洗衣机:容器在漂洗周期中容纳膜,篮子随着容器中的洗涤液移动膜。我们优化了漂洗条件,包括洗涤液的体积、转速、洗涤次数和方向。这种简单的设备使研究人员能够显著提高免疫印迹分析的效率和生产力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Smart Wash: Accelerated Membrane Washing Method in Immunoblot.

Immunoblot, also known as western blot, is a well-established procedure in life science. It is commonly used to determine the relative size and abundance of specific proteins, as well as posttranslational modifications of proteins. While this method is widely employed due to its simplicity, it can take hours or even days to complete. Despite considerable efforts to reduce the overall procedure time, particularly for antibody incubation, the steps involving membrane rinsing have remained unchanged since the development of the immunoblot technique. In this context, we introduce an innovative device called the "Smart Wash," designed to significantly reduce the washing intervals by utilizing a motorized salad spinner. The principle of Smart Wash is akin to that of a household washing machine: the container holds the membranes during the rinsing cycle, and the basket moves the membranes along with the washing solution in the container. We have optimized the rinsing conditions, including the volume of the washing solution, rotation speed, number of washing cycles, and direction. This straightforward device empowers researchers to significantly enhance the efficiency and productivity of immunoblotting analysis.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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