期刊
SENSORS AND ACTUATORS B-CHEMICAL
卷 188, 期 -, 页码 1089-1095出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2013.07.114
关键词
Multi channel screen printed array of electrodes; Streptavidin-alkaline phosphatase; Pencil graphite electrode; miRNA; Magnetic beads; MUX-SPE
资金
- Turkish Scientific and Technological Council (TUBITAK) [110S146]
- Turkish Academy of Sciences (TUBA)
- TUBITAK [110S146]
In the present work, a sensitive and selective enzyme-linked electrochemical sensor technology using magnetic beads assay was demonstrated for voltammetric detection of microRNAs (miRNAs) as the first time herein by using the multi-channel screen-printed array of electrodes (MUX-SPE16s). The streptavidin coated magnetic beads were used as a solid phase to immobilize biotinylated DNA capture probe, and then the complementary target RNA sequence (miRNA-15a) was recognized with the capture DNA probe. After attachment of the streptavidin-alkaline phosphatase enzyme (SALP) to biotinylated hybrid, the electroactive product a-naphthol was measured +0.188 V by linear sweep voltammetry (LSV) technique in combination with a single-use pencil graphite electrode (PGE) compared to MUX-SPE16. The oxidation signal of a-naphthol indicates the hybridization occurred between DNA probe and its RNA target in the sample. The selectivity of our assay was tested in the presence of non-complementary miRNA sequence, a very good discrimination was achieved compared to the results obtained with the full match hybridization of probe with miRNA-15a target. The detection limit of miRNA-15a target sequence was also calculated as 0.992 mu g/mL (98.60 pmole in 1 mL sample) at PGE, and 0.114 mu g/mL (34.20 fmole in 3 mu L sample) with MUX-SPE16 system. 2013 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据