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xMAP Technology: Applications in Detection of Pathogens
xMAP technology is applicable for high-throughput, multiplex and simultaneous detection of different analytes within a single complex sample. xMAP multiplex assays are currently available in various nucleic acid and immunoassay formats, enabling simultaneous detection and typing of pathogenic viruse...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5263158/ https://www.ncbi.nlm.nih.gov/pubmed/28179899 http://dx.doi.org/10.3389/fmicb.2017.00055 |
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author | Reslova, Nikol Michna, Veronika Kasny, Martin Mikel, Pavel Kralik, Petr |
author_facet | Reslova, Nikol Michna, Veronika Kasny, Martin Mikel, Pavel Kralik, Petr |
author_sort | Reslova, Nikol |
collection | PubMed |
description | xMAP technology is applicable for high-throughput, multiplex and simultaneous detection of different analytes within a single complex sample. xMAP multiplex assays are currently available in various nucleic acid and immunoassay formats, enabling simultaneous detection and typing of pathogenic viruses, bacteria, parasites and fungi and also antigen or antibody interception. As an open architecture platform, the xMAP technology is beneficial to end users and therefore it is used in various pharmaceutical, clinical and research laboratories. The main aim of this review is to summarize the latest findings and applications in the field of pathogen detection using microsphere-based multiplex assays. |
format | Online Article Text |
id | pubmed-5263158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52631582017-02-08 xMAP Technology: Applications in Detection of Pathogens Reslova, Nikol Michna, Veronika Kasny, Martin Mikel, Pavel Kralik, Petr Front Microbiol Microbiology xMAP technology is applicable for high-throughput, multiplex and simultaneous detection of different analytes within a single complex sample. xMAP multiplex assays are currently available in various nucleic acid and immunoassay formats, enabling simultaneous detection and typing of pathogenic viruses, bacteria, parasites and fungi and also antigen or antibody interception. As an open architecture platform, the xMAP technology is beneficial to end users and therefore it is used in various pharmaceutical, clinical and research laboratories. The main aim of this review is to summarize the latest findings and applications in the field of pathogen detection using microsphere-based multiplex assays. Frontiers Media S.A. 2017-01-25 /pmc/articles/PMC5263158/ /pubmed/28179899 http://dx.doi.org/10.3389/fmicb.2017.00055 Text en Copyright © 2017 Reslova, Michna, Kasny, Mikel and Kralik. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Reslova, Nikol Michna, Veronika Kasny, Martin Mikel, Pavel Kralik, Petr xMAP Technology: Applications in Detection of Pathogens |
title | xMAP Technology: Applications in Detection of Pathogens |
title_full | xMAP Technology: Applications in Detection of Pathogens |
title_fullStr | xMAP Technology: Applications in Detection of Pathogens |
title_full_unstemmed | xMAP Technology: Applications in Detection of Pathogens |
title_short | xMAP Technology: Applications in Detection of Pathogens |
title_sort | xmap technology: applications in detection of pathogens |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5263158/ https://www.ncbi.nlm.nih.gov/pubmed/28179899 http://dx.doi.org/10.3389/fmicb.2017.00055 |
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