多克隆抗体
检出限
布鲁氏菌
共轭体系
抗体
纳米化学
荧光
量子点
分子生物学
色谱法
一级和二级抗体
细菌
布鲁氏菌病
微生物学
化学
病毒学
生物
材料科学
纳米技术
免疫学
物理
有机化学
量子力学
聚合物
遗传学
作者
Dandan Song,Xiaofeng Qu,Yushen Liu,Li Li,Dehui Yin,Juan Li,Kun Xu,Renguo Xie,Yue Zhai,Huiwen Zhang,Hao Bao,Chao Zhao,Juan Wang,Xiuling Song,Wenzhi Song
标识
DOI:10.1186/s11671-017-1941-z
摘要
Brucella spp. are facultative intracellular bacteria that cause zoonotic disease of brucellosis worldwide. Traditional methods for detection of Brucella spp. take 48-72 h that does not meet the need of rapid detection. Herein, a new rapid detection method of Brucella was developed based on polyclonal antibody-conjugating quantum dots and antibody-modified magnetic beads. First, polyclonal antibodies IgG and IgY were prepared and then the antibody conjugated with quantum dots (QDs) and immunomagnetic beads (IMB), respectively, which were activated by N-(3-dimethylaminopropyl)-N'-ethylcar-bodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS) to form probes. We used the IMB probe to separate the Brucella and labeled by the QD probe, and then detected the fluorescence intensity with a fluorescence spectrometer. The detection method takes 105 min with a limit of detection of 103 CFU/mL and ranges from 10 to 105 CFU/mL (R 2 = 0.9983), and it can be well used in real samples.
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