2011
DOI: 10.1007/978-1-61779-527-5_2
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Detection and Quantification of Cytokines and Other Biomarkers

Abstract: Accurate measurement of cytokine concentrations is a powerful and essential approach to the study of inflammation. The enzyme-linked immunosorbent assay (ELISA) is a simple, low-cost analytical tool that provides both the specificity and sensitivity required for the study of cytokines in vitro or in vivo. This communication describes a systematic approach to develop an indirect sandwich ELISA to detect and quantify cytokines, or other biomarkers, with accuracy and precision. Also detailed is the use of sequent… Show more

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Cited by 75 publications
(51 citation statements)
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“…Images were captured using Quansys Imager, driven by an 8.4 megapixel Canon 20D digital SLR camera, and analyzed using Quansys Software. In order to assure compatibility with measurements of cytokines in previously published studies in the field (Chiswick et al, 2012, Trune et al, 2011, Wong et al, 2008), the antigen standard concentrations used by Quansys (R&D) were referenced to “gold standard” for each cytokine represented on the multiplex plate as previously described (Lattie, Antoni, 2012). …”
Section: Methodsmentioning
confidence: 99%
“…Images were captured using Quansys Imager, driven by an 8.4 megapixel Canon 20D digital SLR camera, and analyzed using Quansys Software. In order to assure compatibility with measurements of cytokines in previously published studies in the field (Chiswick et al, 2012, Trune et al, 2011, Wong et al, 2008), the antigen standard concentrations used by Quansys (R&D) were referenced to “gold standard” for each cytokine represented on the multiplex plate as previously described (Lattie, Antoni, 2012). …”
Section: Methodsmentioning
confidence: 99%
“…The most common approach for cytokine quantification is based on the idea of an immunoassay. Specific techniques include traditional ELISA assays, (Chiswick et al 2012) enzyme-linked immunosorbent spot (ELIspot) assays, (Cox et al 2006) antibody array assays (Schröder et al 2010) and bead-based assays (Won et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…[30] Proinflammatory cytokines, particularly interleukin 1 (IL-1) and tumor necrosis factor alpha (TNF-b) upregulated during the inflammatory process. [31] The standard enzyme-linked immunosorbent assay method was used for analyzing quantification of FGF, TGF-b1, IL-1 alpha (IL-1a), VEGF, TNF-a, plateletderived growth factor (PDGF) and caspase 3 (CASP3) cytokines [32] to evaluate the effect of MSCs in the infected tissue samples.…”
Section: Methodsmentioning
confidence: 99%