检出限
免疫分析
多克隆抗体
分析物
噬菌体
色谱法
介电谱
化学
材料科学
抗体
电极
电化学
生物
大肠杆菌
生物化学
基因
物理化学
免疫学
作者
Madhavi Pali,Candace S. Bever,Natalia Vasylieva,Bruce D. Hammock,Ian Ivar Suni
标识
DOI:10.1002/elan.201800457
摘要
Abstract Both direct and non‐competitive two‐site (sandwich) immunoassays are reported for 3‐phenoxybenzoic acid (3‐PBA) utilizing signal transduction by electrochemical impedance spectroscopy (EIS), and the sandwich immunoassay reduces the detection limit for this small molecule analyte by ∼70×. The direct EIS immunoassay utilizes a polyclonal antibody to 3PBA for biomolecular recognition, while the sandwich EIS immunoassay utilizes in addition a previously reported antiimmunocomplex M13 bacteriophage clone. For both immunoassays, the polyclonal antibody film is immobilized atop an Au electrode by amide bond formation. The direct EIS immunoassay exhibits a 3‐PBA sensitivity of 5.4×10 4 kΩ cm 2 M 1 , and a detection limit of 2.5×10 −4 M (54 μg/ml), while the sandwich EIS immunoassay exhibits a 3PBA sensitivity of 4.2×10 6 kΩ cm 2 M −1 , and a detection limit of 3.4×10 −6 M (0.74 μg/ml). For the sandwich EIS immunoassay, a constant excess (80×10 9 PFU/ml) of bacteriophage is maintained during all experiments. This is the first report of a bacteriophage‐assisted sandwich EIS assay.
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