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A microfluidic dual-well device for high-throughput single-cell capture and culture

机译:用于高通量单细胞捕获和培养的微流控双孔设备

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In vitro culture of single cells facilitates biological studies by deconvoluting complications from cell population heterogeneity. However, there is still a lack of simple yet high-throughput methods to perform single cell culture experiments. In this paper, we report the development and application of a microfluidic device with a dual-well (DW) design concept for high-yield single-cell loading (similar to 77%) in large microwells (285 and 485 mu m in diameter) which allowed for cell spreading, proliferation and differentiation. The increased single-cell loading yield is achieved by using sets of small microwells termed "capture-wells" and big microwells termed "culture-wells" according to their utilities for single-cell capture and culture, respectively. This novel device architecture allows the size of the "culture" microwells to be flexibly adjusted without affecting the single-cell loading efficiency making it useful for cell culture applications as demonstrated by our experiments of KT98 mouse neural stem cell differentiation, A549 and MDA-MB-435 cancer cell proliferation, and single-cell colony formation assay with A549 cells in this paper.
机译:通过从细胞群体异质性中解开复杂性,单细胞的体外培养有助于生物学研究。但是,仍然缺乏执行单细胞培养实验的简单而高通量的方法。在本文中,我们报告了具有双孔(DW)设计概念的微流控设备的开发和应用,该设计概念可用于大型微孔(直径285和485μm)中的高产量单细胞上样(约占77%)它可以使细胞扩散,增殖和分化。根据分别用于单细胞捕获和培养的效用,分别使用称为“捕获孔”的小微孔和称为“培养孔”的大微孔,可以提高单细胞负载量。这种新颖的设备架构可灵活调整“培养”微孔的大小,而不会影响单细胞加载效率,从而使其可用于细胞培养,如我们的KT98小鼠神经干细胞分化实验,A549和MDA-MB所证明的那样本文研究了-435癌细胞的增殖以及使用A549细胞进行单细胞集落形成的方法。

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