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A Single Cells Patterning Approach for Human Promyelocytic Leukemia Cells

机译:人类早幼粒细胞白血病细胞的单细胞模式化方法

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摘要

To get the detailed information of single cells and screen drugs effectively,especially to develop anti-cancer drugs in view of the cellular heterogeneity of tumors,biochips on single-cell level are necessary.Based on the fabrication techniques of MEMS,substrates with areas of hydrophilicity and hydrophobicity were fabricated to pattern single cells.The optimal process parameters for substrates fabrication are obtained through a series of experiments.MEMS substrates with clear binary surface patterns of hydrophilicity and hydrophobicity are achieved and a general streptavidin template with high bio-compatibility was prepared.In the experiment,biotin-BSA was employed as adhesive proteins Followed by streptavidin and biotinylated antibodies.An array of single HL-60 (Human Promyelocytic Leukemia Cells,HL-60) cells was obtained based on above protein adsorption substrate.The factors affecting the result of the single-cells patterning were investigated and optimized,by which a relatively high patterning rate is achieved.To keep cells characteristics and also for the future parallel patterning of different cells,specific antibodies are investigated for the cell HL-60,including CD45 and CD15.The result of antibodies immobilization and patterning are presented,which can well match the designed template.
机译:为了获得单细胞的详细信息并筛选药物,特别是鉴于肿瘤的细胞异质性,开发抗癌药物,必须在单细胞水平上使用生物芯片。基于MEMS的制造技术,具有通过一系列实验获得了亲水性和疏水性以构图单个细胞的最佳工艺参数,获得了具有清晰的亲水性和疏水性二元表面图案的MEMS基底,并制备了具有高生物相容性的通用链霉亲和素模板在实验中,以生物素-BSA作为黏附蛋白,接着是链霉亲和素和生物素化抗体。基于上述蛋白吸附底物,获得了一系列单个HL-60(人类早幼粒细胞白血病细胞,HL-60)细胞。对单细胞构图的结果进行了研究和优化,相对而言为保持gh图案化速率。为了保持细胞特性以及将来对不同细胞进行平行图案化,研究了HL-60细胞的特异性抗体,包括CD45和CD15。提出了抗体固定和图案化的结果,可以很好地实现匹配设计的模板。

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