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Improvement for gene transfection of bacteria using magnetic attraction

机译:利用磁吸引力改善细菌的基因转染

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We propose cells can be descended using magnetic attraction, which leads to shorter experimental time and higher efficiency. We used an electroporation chip with adjustable electromagnetic field as the experimental platform, and tested Escherichia coli and 6-nm magnetic beads combined with DNA plasmid. The magnetic beads were positively charged and easy to bind to the negatively charged cell membrane of E. coli. The magnetic beads and E. coli could be attracted quickly to the bottom because of the electromagnet and could reduce operational time and enhance transfection efficiency. After electroporating and culturing, we obtained the results for E. coli with drug resistance and calculated the number of colony as the transfection efficiency. The achieved transfection efficiency using magnetic beads was seven-fold higher than that without magnetic bead. The following optimum parameter values were determined: 1.4 × 1014 bead/ml for nano-magnetic bead concentration, 200 Gauss for magnetic flux density, and 40 s for magnetic attraction lasting time. The results will help develop transfection applications for low-descent-velocity cells.
机译:我们提出电池可以使用磁吸引力下降,这导致了更短的实验时间和更高的效率。我们使用具有可调节电磁场的电穿孔芯片作为实验平台,并测试大肠杆菌和6-NM磁珠与DNA质粒联合。磁珠被带正电荷且易于与大肠杆菌的带负电荷的细胞膜结合。由于电磁铁,磁珠和大肠杆菌可以快速吸引到底部,并且可以降低运行时间并增强转染效率。在电穿孔和培养后,我们通过耐药性获得了大肠杆菌的结果,并计算了作为转染效率的菌落数量。使用磁珠实现的转染效率比没有磁珠的七倍高。确定以下最佳参数值:1.4×1014珠/ mL,用于纳米磁性珠粒浓度,磁通密度200的高斯,磁力吸引持续时间为40秒。结果将有助于开发用于低压速度细胞的转染应用。

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