中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Developing A Microfluidic-Based System To Quantify Cell Capture Efficiency

文献类型:期刊论文

作者Yang F(杨帆); Gao YX(高宇欣); Zhang Y(章燕); Chen J(陈娟); Long M(龙勉); Long M
刊名Science in China Series C-Life Sciences
出版日期2009
卷号52期号:2页码:173-181
通讯作者邮箱mlong@imech.ac.cn
ISSN号1006-9305
关键词Cell Surface Marker Microfluidic Capture Efficiency Ligand Binding-Kinetics Antibody Microarray Surface-Antigens Leukemias Identification Diagnostics Membrane Platform Design Marker
通讯作者Long M
中文摘要Micro-fabrication technology has substantial potential for identifying molecular markers expressed on the surfaces of tissue cells and viruses. It has been found in several conceptual prototypes that cells with such markers are able to be captured by their antibodies immobilized on microchannel substrates and unbound cells are flushed out by a driven flow. The feasibility and reliability of such a microfluidic-based assay, however, remains to be further tested. In the current work, we developed a microfluidic-based system consisting of a microfluidic chip, an image grabbing unit, data acquisition and analysis software, as well as a supporting base. Specific binding of CD59-expressed or BSA-coupled human red blood cells (RBCs) to anti-CD59 or anti-BSA antibody-immobilized chip surfaces was quantified by capture efficiency and by the fraction of bound cells. Impacts of respective flow rate, cell concentration, antibody concentration and site density were tested systematically. The measured data indicated that the assay was robust. The robustness was further confirmed by capture efficiencies measured from an independent ELISA-based cell binding assay. These results demonstrated that the system developed provided a new platform to effectively quantify cellular surface markers effectively, which promoted the potential applications in both biological studies and clinical diagnoses.
类目[WOS]Biology
研究领域[WOS]Life Sciences & Biomedicine - Other Topics
关键词[WOS]LIGAND BINDING-KINETICS ; ANTIBODY MICROARRAY ; SURFACE-ANTIGENS ; LEUKEMIAS ; IDENTIFICATION ; DIAGNOSTICS ; MEMBRANE ; PLATFORM ; DESIGN ; MARKER
收录类别SCI
语种英语
WOS记录号WOS:000264106000017
公开日期2009-08-03 ; 2009-10-09
源URL[http://dspace.imech.ac.cn/handle/311007/26718]  
专题力学研究所_国家微重力实验室
通讯作者Long M
推荐引用方式
GB/T 7714
Yang F,Gao YX,Zhang Y,et al. Developing A Microfluidic-Based System To Quantify Cell Capture Efficiency[J]. Science in China Series C-Life Sciences,2009,52(2):173-181.
APA 杨帆,高宇欣,章燕,陈娟,龙勉,&Long M.(2009).Developing A Microfluidic-Based System To Quantify Cell Capture Efficiency.Science in China Series C-Life Sciences,52(2),173-181.
MLA 杨帆,et al."Developing A Microfluidic-Based System To Quantify Cell Capture Efficiency".Science in China Series C-Life Sciences 52.2(2009):173-181.

入库方式: OAI收割

来源:力学研究所

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