首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Fluorescence quantification of intracellular materials at the single-cell level by an integrated dual-well array microfluidic device
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Fluorescence quantification of intracellular materials at the single-cell level by an integrated dual-well array microfluidic device

机译:通过集成双孔阵列微流体装置在单细胞水平下细胞内材料的荧光定量

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摘要

We present an integrated microfluidic device for quantifying intracellular materials at the single-cell level. This device combines a dual-well structure and a microfluidic control system. The dual-well structure includes capture wells (20 m in diameter) for trapping a single cell and reaction wells (200 m in diameter) for confining reagents. The control system enables a programmable procedure for single-cell analysis. This device achieves highly efficient trapping of single cells, overcoming the Poisson distribution, while affording sufficient biochemical reagents for each isolated reactor. We successfully utilized the presented device to monitor the catalytic interaction between intracellular alkaline phosphatase enzyme and a fluorogenic substrate and to quantify the intracellular glucose concentration of a single K562 cell based on an external standard method. The results demonstrate the feasibility and convenience of our dual-well array microfluidic device as a practical single-cell research tool.
机译:我们介绍了一种用于定量单细胞水平的细胞内材料的集成微流体装置。该装置结合了双井结构和微流体控制系统。双阱结构包括捕获孔(直径为20μm),用于捕获单个电池和反应孔(直径为200μm),用于限制试剂。控制系统使单个小区分析能够可编程过程。该装置实现了对单细胞的高效诱捕,克服泊松分布,同时为每个分离的反应器提供足够的生化试剂。我们成功地利用所提出的装置监测细胞内碱性磷酸酶和荧光基质之间的催化相互作用,并基于外标方法量化单个K562电池的细胞内葡萄糖浓度。结果证明了我们双井阵列微流体装置作为实用单细胞研究工具的可行性和便利性。

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