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首页> 外文期刊>Advances in Experimental Medicine and Biology >Combining the 'Sibling Technologies' of Laser Capture Microdissection and Reverse Phase Protein Microarrays
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Combining the 'Sibling Technologies' of Laser Capture Microdissection and Reverse Phase Protein Microarrays

机译:结合激光捕获微量碎裂和反相蛋白质微阵列的“兄弟姐妹技术”

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Reverse phase protein microarrays (RPPA) and laser capture microdissection (LCM) are "sibling" technologies that originated from the same laboratory to overcome the challenge of quantifying low-abundance proteins in heterogeneous tissues. Combining both technologies provides both unique opportunities and unique challenges. Enabling the unprecedented resolution of the activation state of labile biomarkers, such as phosphorylated cell signaling proteins, has had a substantial impact on our understanding of diseases and is playing a significant role in clinical trials. At the same time, quantifying proteins at this sensitivity in very small amounts of material requires cognizance of pre-analytical variability and the limits of downstream detection technologies. Here, we discuss both the potential that the combination of both technologies presents and the potential pitfalls that must be navigated.
机译:反相蛋白质微阵列(RPPA)和激光捕获微粉(LCM)是源自同一实验室的“兄弟”技术,以克服在异质组织中定量低丰度蛋白的挑战。 组合两种技术都提供了独特的机会和独特的挑战。 能够实现不稳定的稳定生物标志物的激活状态,例如磷酸化的细胞信号传导蛋白,对我们对疾病的理解具有大量影响,并在临床试验中发挥着重要作用。 同时,在非常少量的材料中以这种敏感度定量蛋白质需要认识到预分析变异性和下游检测技术的限制。 在这里,我们讨论两种技术的组合存在的潜力和必须导航的潜在陷阱。

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