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首页> 外文期刊>Cytometry, Part A: the journal of the International Society for Analytical Cytology >Development of a bead-based multiplex assay for the simultaneous detection of porcine inflammation markers using xMAP technology
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Development of a bead-based multiplex assay for the simultaneous detection of porcine inflammation markers using xMAP technology

机译:基于珠的多重分析技术的开发,用于使用xMAP技术同时检测猪的炎症标志物

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摘要

Commercially available assays for the simultaneous detection of multiple inflammatory and cardiac markers in porcine blood samples are currently lacking. Therefore, this study was aimed at developing a bead-based, multiplexed flow cytometric assay to simultaneously detect porcine cytokines [interleukin (IL)-1β, IL-6, IL-10, and tumor necrosis factor alpha], chemokines (IL-8 and monocyte chemotactic protein 1), growth factors [basic fibroblast growth factor (bFGF), vascular endothelial growth factor, and platelet-derived growth factor-bb], and injury markers (cardiac troponin-I) as well as complement activation markers (C5a and sC5b-9). The method was based on the Luminex xMAP technology, resulting in the assembly of a 6- and 11-plex from the respective individual singleplex situation. The assay was evaluated for dynamic range, sensitivity, cross-reactivity, intra-assay and interassay variance, spike recovery, and correlation between multiplex and commercially available enzyme-linked immunosorbent assay as well as the respective singleplex. The limit of detection ranged from 2.5 to 30,000 pg/ml for all analytes (6- and 11-plex assays), except for soluble C5b-9 with a detection range of 2-10,000 ng/ml (11-plex). Typically, very low cross-reactivity (<3% and <1.4% by 11- and 6-plex, respectively) between analytes was found. Intra-assay variances ranged from 4.9 to 7.4% (6-plex) and 5.3 to 12.9% (11-plex). Interassay variances for cytokines were between 8.1 and 28.8% (6-plex) and 10.1 and 26.4% (11-plex). Correlation coefficients with singleplex assays for 6-plex as well as for 11-plex were high, ranging from 0.988 to 0.997 and 0.913 to 0.999, respectively. In this study, a bead-based porcine 11-plex and 6-plex assay with a good assay sensitivity, broad dynamic range, and low intra-assay variance and cross-reactivity was established. These assays therefore represent a new, useful tool for the analysis of samples generated from experiments with pigs.
机译:当前缺乏用于同时检测猪血样中多种炎症和心脏标志物的商业化检测方法。因此,本研究旨在开发一种基于微珠的多重流式细胞术,以同时检测猪细胞因子[白介素(IL)-1β,IL-6,IL-10和肿瘤坏死因子α],趋化因子(IL-8和单核细胞趋化蛋白1),生长因子[碱性成纤维细胞生长因子(bFGF),血管内皮生长因子和血小板衍生的生长因子bb],损伤标记物(心肌肌钙蛋白I)以及补体激活标记物(C5a和sC5b-9)。该方法基于Luminex xMAP技术,可根据各自的单重态情况组装6和11重。评价该测定的动态范围,灵敏度,交叉反应性,测定内和测定间差异,加标回收率以及多重分析和可商购的酶联免疫吸附测定以及相应的单重分析之间的相关性。对于所有分析物(6-和11-plex分析),检测限范围为2.5至30,000 pg / ml,除了可溶性C5b-9的检测范围为2-10,000 ng / ml(11-plex)。通常,发现分析物之间的交叉反应性非常低(分别通过11和6络合物分别<3%和<1.4%)。测定内方差范围为4.9%至7.4%(6重)和5.3%至12.9%(11重)。细胞因子的测定间差异在8.1和28.8%(6重)和10.1和26.4%(11重)之间。 6重和11重的单重测定相关系数很高,分别为0.988至0.997和0.913至0.999。在这项研究中,建立了基于珠子的猪11重和6重测定法,具有良好的测定灵敏度,宽动态范围,低测定内差异和交叉反应性。因此,这些测定法代表了一种新的,有用的工具,可用于分析猪实验产生的样品。

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