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首页> 外文期刊>Methods: A Companion to Methods in Enzymology >LC3-and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells
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LC3-and p62-based biochemical methods for the analysis of autophagy progression in mammalian cells

机译:基于LC3和p62的生化方法用于分析哺乳动物细胞中自噬的进程

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摘要

Autophagy is an intracellular degradation system that delivers cytoplasmic materials to the lysosome or vacuole. This system plays a crucial role in various physiological and pathological processes in living organisms ranging from yeast to mammals. Thus, an accurate and reliable measure of autophagic activity is necessary. However, autophagy involves dynamic and complicated processes that make it difficult to analyze. The term "autophagic flux" is used to denote overall autophagic degradation (i.e., delivery of autophagic cargo to the lysosome) rather than autophagosome formation. Immunoblot analysis of LC3 and p62/SQSTM1, among other proteins, has been widely used to monitor autophagic flux. Here, we describe basic protocols to measure the levels of endogenous LC3 and p62 by immunoblotting in cultured mammalian cells. (C) 2014 Elsevier Inc. All rights reserved.
机译:自噬是一种细胞内降解系统,可将细胞质物质输送至溶酶体或液泡。该系统在从酵母到哺乳动物的活生物体的各种生理和病理过程中都起着至关重要的作用。因此,需要准确可靠的自噬活性测量方法。但是,自噬涉及动态且复杂的过程,因此很难进行分析。术语“自噬通量”用于表示整体自噬降解(即,将自噬货物递送至溶酶体)而不是自噬体形成。 LC3和p62 / SQSTM1以及其他蛋白质的免疫印迹分析已广泛用于监测自噬通量。在这里,我们描述了通过在培养的哺乳动物细胞中进行免疫印迹来测量内源性LC3和p62的水平的基本协议。 (C)2014 Elsevier Inc.保留所有权利。

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