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Microflow Cytometry in Studies of Programmed Tumour Cell Death

机译:微射线细胞测定法在编程肿瘤细胞死亡中的研究中

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Flow cytometry is one of the core technologies for a single cell analysis and sorting based on fluorescent markers and functional probes. Nevertheless, popular adoption and proliferation of this technology is still limited by the high cost, need for dedicated personnel, lack of miniaturization and requirement for considerable sample volumes. In this work we demonstrate that advanced multiparameter assays to track the caspase-dependent cell death can be rapidly performed using innovative microfluidic flow cytometry (μFCM). This enabling technology features a user-friendly chip-based system integrated with the dedicated off-chip electronic interface. It can perform multivariate analysis using sampling volumes as small as 10 microlitres. We for the first time present evidence that microfluidic flow cytometry can be used to resolve the DNA content and track the pharmacologically induced activation of caspases and dissipation of mitochondrial inner membrane potential (ΔΨm) in relation to the cell cycle in living human tumor cells.
机译:流式细胞术是基于荧光标记和功能探针的单细胞分析和分选的核心技术之一。尽管如此,本技术的流行采用和扩散仍然受到高成本的限制,需要专用人员,缺乏小型化和可观的样本量的要求。在这项工作中,我们证明了使用创新的微流体流式细胞术(μFCM)可以快速进行追踪依赖依赖性细胞死亡的先进的多分钟测定。这种启用技术采用了一种基于用户友好的基于芯片的系统,与专用的片外电子接口集成。它可以使用小于10微升的抽样量来执行多变量分析。我们首次出现的证据表明,微流体流式细胞术可用于解析DNA含量并追踪药物诱导的胱天蛋白酶的活化和线粒体内膜电位(Δψm)的散发,与活性人肿瘤细胞中的细胞周期相关。

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