微流控
限制
封装(网络)
细胞
材料科学
下降(电信)
单细胞分析
化学
细胞包封
纳米技术
计算机科学
工程类
机械工程
生物化学
计算机网络
电信
作者
Luoquan Li,Ping Wu,Zhaofeng Luo,Lei Wang,Weiping Ding,Tao Wu,Jinyu Chen,Jinlong He,Yi He,Heran Wang,Ying Chen,Guibo Li,Zida Li,Liqun He
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2019-05-02
卷期号:4 (5): 1299-1305
被引量:37
标识
DOI:10.1021/acssensors.9b00171
摘要
Droplet microfluidics-based platform (Drop-seq) has been shown to be a powerful tool for single cell expression profiling. Nevertheless, this platform required the simultaneous encapsulation of single cell and single barcoded bead, the incidence of which was very low, limiting its efficiency. Spiral channels were reported to focus the barcoded beads and thus increased the efficiency, but focusing of cells was not demonstrated, which could potentially further enhance the performance. Here, we designed spiral and serpentine channels to focus both bead and cell solutions and implemented this microfluidic design on Drop-seq. We characterized the effect of cell/bead concentration on encapsulation results and tested the performance by coencapsulating barcoded beads and human–mouse cell mixtures followed by sequencing. The results showed ∼300% and ∼40% increase in cell utilization rate compared to the traditional Drop-seq device and the device focusing beads alone, respectively. This chip design showed great potential for high efficiency single cell expression profiling.
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