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Capillary Electrophoresis with Electrochemiluminescent Detection for Highly Sensitive Assay of Genetically Modified Organisms
被引:29
|作者:
Guo, Longhua
[1
,2
]
Yang, Huanghao
[1
]
Qiu, Bin
[1
]
Xiao, Xueyang
[1
]
Xue, Linlin
[1
]
Kim, Donghwan
[2
]
Chen, Guonan
[1
]
机构:
[1] Fuzhou Univ, Minist Educ, Key Lab Anal & Detect Food Safety, Fujian Prov Key Lab Anal & Detect Food Safety,Dep, Fuzhou 350002, Peoples R China
[2] Nanyang Technol Univ, Div Bioengn, Sch Chem & Biomed Engn, Singapore 637457, Singapore
关键词:
END-COLUMN ELECTROCHEMILUMINESCENCE;
POLYMERASE-CHAIN-REACTION;
ELECTROGENERATED CHEMILUMINESCENCE;
FLUORESCENCE DETECTION;
GEL-ELECTROPHORESIS;
MODIFIED MAIZE;
HUMAN URINE;
MICROCHIP;
SEPARATION;
SYSTEM;
D O I:
10.1021/ac901510s
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A capillary electrophoresis coupled with electrochemiluminescent detection system (CE-ECL) was developed for the detection of polymerase chain reaction (PCR) amplicons. The ECL luminophore, tris(1,10-phenanthroline) ruthenium(II) (Ru(phen)(3)(2+)), was labeled to the PCR primers before amplification. Ru(phen)(3)(2+) Was then introduced to PCR amplicons by PCR amplification. Eventually, the PCR amplicons were separated and detected by the homemade CE-ECL system. The detection of a typical genetically modified organism (GMO), Roundup Ready Soy (RRS), was shown as an example to demonstrate the reliability of the proposed approach. Four pairs of primers were amplified by multiple PCR (MPCR) simultaneously, three of which were targeted on the specific sequence of exogenous genes of RRS, and another was targeted on the endogenous reference gene of soybean. Both the conditions for PCR amplification and CE-ECL separation and detection were investigated in detail. Results showed that, under the optimal conditions, the proposed method can accurately identifying RRS. The corresponding limit of detection (LOD) was below 0.01% with 35 PCR cycles.
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页码:9578 / 9584
页数:7
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