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一种基于磁珠的快速灵敏免疫分析法,用于检测葡萄球菌肠毒素B以进行高通量筛选。

A rapid and sensitive magnetic bead-based immunoassay for the detection of staphylococcal enterotoxin B for high-through put screening.

作者信息

Alefantis Tim, Grewal Paul, Ashton John, Khan Akbar S, Valdes James J, Del Vecchio Vito G

机构信息

Vital Probes, Inc., 1300 Old Plank Road, Mayfield, PA 18433, USA.

出版信息

Mol Cell Probes. 2004 Dec;18(6):379-82. doi: 10.1016/j.mcp.2004.06.003.

Abstract

Staphylococcal enterotoxin B (SEB) is one of many toxins produced by the Gram-positive bacterium Staphylococcal aureus. While SEB is known as the causative agent of certain food poisonings it is also considered a biological Select Agent. Thus, rapid and accurate identification of SEB during either surveillance or in response to a biothreat is critical to the mitigation of the suspect agent. This report presents an improved method for the detection of SEB based on a SEB-specific, two-antibody system where one antibody was bound to a magnetic bead particle while the other was labeled with Alexa fluor 647. The assay consisted of one incubation period for 30 minutes where all reagents necessary to detect SEB were included. Using this assay 100 pg of recombinant purified SEB, as well as SEB from the culture supernatant of several strains of methicillin-resistant S. aureus were detected with fidelity. This assay presents improvements over current assays in terms of a combination of the reduction in assay time length, assay sensitivity, ease of use, and application to automated high-throughput analysis. Additionally, this assay can be easily modified to detect a wide range of proteins and whole organisms.

摘要

葡萄球菌肠毒素B(SEB)是革兰氏阳性菌金黄色葡萄球菌产生的多种毒素之一。虽然SEB是某些食物中毒的病原体,但它也被视为一种生物选择剂。因此,在监测期间或应对生物威胁时快速准确地鉴定SEB对于减轻可疑病原体至关重要。本报告介绍了一种基于SEB特异性双抗体系统检测SEB的改进方法,其中一种抗体与磁珠颗粒结合,另一种抗体用Alexa fluor 647标记。该检测包括一个30分钟的孵育期,其中包含检测SEB所需的所有试剂。使用该检测方法,可准确检测出100 pg重组纯化的SEB以及几种耐甲氧西林金黄色葡萄球菌菌株培养上清液中的SEB。该检测方法在检测时间缩短、检测灵敏度、易用性以及应用于自动化高通量分析等方面比现有检测方法有所改进。此外,该检测方法可轻松修改以检测多种蛋白质和完整生物体。

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