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基于商业荧光微球的Luminex细胞因子检测的评估。

An evaluation of commercial fluorescent bead-based luminex cytokine assays.

作者信息

Djoba Siawaya Joel Fleury, Roberts Teri, Babb Chantal, Black Gillian, Golakai Hawa Jande, Stanley Kim, Bapela Nchinya Bennedict, Hoal Eileen, Parida Shreemanta, van Helden Paul, Walzl Gerhard

机构信息

Department of Biomedical Sciences, Division of Molecular Biology and Human Genetics, Stellenbosch University Cape-Town, Stellenbosch, South Africa.

出版信息

PLoS One. 2008 Jul 2;3(7):e2535. doi: 10.1371/journal.pone.0002535.

Abstract

The recent introduction of fluorescent bead-based technology, allowing the measurement of multiples analytes in a single 25-50 microl sample has revolutionized the study of cytokine responses. However, such multiplex approaches may compromise the ability of these assays to accurately measure actual cytokine levels. This study evaluates the performance of three commercially available multiplex cytokine fluorescent bead-based immunoassays (Bio-Rad's Cytokine 17-plex kit; LINCO Inc's 29-plex kit; and RnD System's Fluorokine-Multi Analyte Profiling (MAP) base kit A and B). The LINCO Inc kit was found to be the most sensitive assay for measuring concentrations of multiple recombinant cytokines in samples that had been spiked with serial dilutions of the standard provided by the manufacturer, followed respectively by the RnD Fluorokine-(MAP) and Bio-Rad 17-plex kits. A positive correlation was found in the levels of IFN-gamma measured in antigen stimulated whole blood culture supernatants by the LINCO Inc 29-plex, RnD Fluorokine-(MAP) and RnD system IFN-gamma Quantikine ELISA kits across a panel of controls and stimulated samples. Researchers should take the limitation of such multiplexed assays into account when planning experiments and the most appropriate use for these tests may currently be as screening tools for the selection of promising markers for analysis by more sensitive techniques.

摘要

最近引入的基于荧光微珠的技术,能够在25 - 50微升的单个样本中检测多种分析物,这彻底改变了细胞因子反应的研究。然而,这种多重检测方法可能会影响这些检测准确测量实际细胞因子水平的能力。本研究评估了三种市售的基于荧光微珠的多重细胞因子免疫分析方法(伯乐公司的细胞因子17种分析物试剂盒;LINCO公司的29种分析物试剂盒;以及RnD系统的荧光细胞因子 - 多分析物检测(MAP)基础试剂盒A和B)。研究发现,在对制造商提供的标准品进行系列稀释后添加到样本中的情况下,LINCO公司的试剂盒对于测量多种重组细胞因子的浓度最为灵敏,其次分别是RnD荧光细胞因子 -(MAP)试剂盒和伯乐公司的17种分析物试剂盒。在一组对照和刺激样本中,通过LINCO公司的29种分析物试剂盒、RnD荧光细胞因子 -(MAP)试剂盒以及RnD系统的IFN -γ定量酶联免疫吸附测定试剂盒,在抗原刺激的全血培养上清液中测得的IFN -γ水平之间发现了正相关。研究人员在规划实验时应考虑此类多重检测的局限性,并且目前这些检测最合适的用途可能是作为筛选工具,用于选择有前景的标志物,以便通过更灵敏的技术进行分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cb9/2432042/9f267701c045/pone.0002535.g001.jpg

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