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A simple, sensitive and selective quantum-dot-based western blot method for the simultaneous detection of multiple targets from cell lysates

机译:一种简单,灵敏且选择性的基于量子点的蛋白质印迹方法,可同时检测细胞裂解物中的多个靶标

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摘要

Quantum dots (Qdots) are fluorescent nanoparticles that have great potential as detection agents in biological applications. Their optical properties, including photostability and narrow, symmetrical emission bands with large Stokes shifts, and the potential for multiplexing of many different colours, give them significant advantages over traditionally used fluorescent dyes. Here, we report the straightforward generation of stable, covalent quantum dot-protein A/G bioconjugates that will be able to bind to almost any IgG antibody, and therefore can be used in many applications. An additional advantage is that the requirement for a secondary antibody is removed, simplifying experimental design. To demonstrate their use, we show their application in multiplexed western blotting. The sensitivity of Qdot conjugates is found to be superior to fluorescent dyes, and comparable to, or potentially better than, enhanced chemiluminescence. We show a true biological validation using a four-colour multiplexed western blot against a complex cell lysate background, and have significantly improved previously reported non-specific binding of the Qdots to cellular proteins.
机译:量子点(Qdots)是荧光纳米颗粒,在生物应用中作为检测剂具有巨大潜力。它们的光学特性(包括光稳定性和具有大斯托克斯位移的狭窄,对称的发射带)以及多种不同颜色的复用潜力使它们比传统使用的荧光染料更具优势。在这里,我们报告了稳定,共价量子点蛋白A / G生物缀合物的直接产生,该缀合物将能够与几乎任何IgG抗体结合,因此可以用于许多应用中。另一个优点是消除了对第二抗体的需求,从而简化了实验设计。为了证明其用途,我们展示了它们在多重蛋白质印迹中的应用。发现Qdot共轭物的灵敏度优于荧光染料,与增强的化学发光相当,甚至可能更好。我们展示了针对复杂的细胞裂解物背景使用四色多重蛋白质印迹的真实生物学验证,并且已经大大改善了Qdots对细胞蛋白的非特异性结合。

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