کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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867073 | 1470989 | 2013 | 5 صفحه PDF | دانلود رایگان |

A DNA-labeled immunosensor for melamine (MEL) detection is presented which combined the exponential amplification and quantitative effect of Real-Time quantitative PCR (RT-qPCR) with the simplicity and specificity of competitive antigen–antibody reaction. An excellent linear relationship between cycle threshold (Ct) and MEL concentration in the range of 0.001–10 pg g−1 was obtained with a limit of detection of 0.3 fg g−1. Compared with other methods, the sensitivity of this DNA-labeled immunosensor showed a 1000-fold improvement, and was below the strictest safety limit of 1 ppm. Furthermore, the specificity was excellent and the recovery in liquid milk samples spiked with MEL was satisfactory. With the advantages of high sensitivity and a low limit of detection (LOD), this sensor is a powerful and promising tool for the detection of other small molecules besidesMEL.
► A DNA-labeled immunosensor for detection of melamine based on PCR amplification was developed.
► The sensor could achieve a low limit of detection of 0.3 fg g−1 in the range of 0.001–10 pg g−1.
► The results showed the simple operations and high-throughput detections.
Journal: Biosensors and Bioelectronics - Volume 42, 15 April 2013, Pages 51–55