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Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry
Recent advances in flow cytometry instrumentation and fluorochrome chemistries have greatly increased fluorescent conjugated antibody combinations that can be used reliably and easily in routine experiments. The Cytek Aurora flow cytometer was first released with three excitation lasers (405, 488, a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790705/ https://www.ncbi.nlm.nih.gov/pubmed/35112484 http://dx.doi.org/10.1002/cyto.a.24537 |
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author | Seong, Yekyung Nguyen, Denny X Wu, Yian Thakur, Archana Harding, Fiona Nguyen, Tuan Andrew |
author_facet | Seong, Yekyung Nguyen, Denny X Wu, Yian Thakur, Archana Harding, Fiona Nguyen, Tuan Andrew |
author_sort | Seong, Yekyung |
collection | PubMed |
description | Recent advances in flow cytometry instrumentation and fluorochrome chemistries have greatly increased fluorescent conjugated antibody combinations that can be used reliably and easily in routine experiments. The Cytek Aurora flow cytometer was first released with three excitation lasers (405, 488, and 640 nm) and incorporated the latest Avalanche Photodiode (APD) technology, demonstrating significant improvement in sensitivity for fluorescent emission signals longer than 800 nm. However, there are limited commercially available fluorochromes capable of excitation with peak emission signals beyond 800 nm. To address this gap, we engineered six new fluorochromes: PE‐750, PE‐800, PE‐830 for the 488 nm laser and APC‐750, APC‐800, APC‐830 for the 640 nm laser. Utilizing the principal of fluorescence resonance energy transfer (FRET), these novel structures were created by covalently linking a protein donor dye with an organic small molecule acceptor dye. Additionally, each of these fluorochrome conjugates were shown to be compatible with fixation/permeabilization buffer reagents, and demonstrated acceptable brightness and stability when conjugated to antigen‐specific monoclonal antibodies. These six novel fluorochrome reagents can increase the numbers of fluorochromes that can be used on a spectral flow cytometer. |
format | Online Article Text |
id | pubmed-9790705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97907052022-12-28 Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry Seong, Yekyung Nguyen, Denny X Wu, Yian Thakur, Archana Harding, Fiona Nguyen, Tuan Andrew Cytometry A Technical Note Recent advances in flow cytometry instrumentation and fluorochrome chemistries have greatly increased fluorescent conjugated antibody combinations that can be used reliably and easily in routine experiments. The Cytek Aurora flow cytometer was first released with three excitation lasers (405, 488, and 640 nm) and incorporated the latest Avalanche Photodiode (APD) technology, demonstrating significant improvement in sensitivity for fluorescent emission signals longer than 800 nm. However, there are limited commercially available fluorochromes capable of excitation with peak emission signals beyond 800 nm. To address this gap, we engineered six new fluorochromes: PE‐750, PE‐800, PE‐830 for the 488 nm laser and APC‐750, APC‐800, APC‐830 for the 640 nm laser. Utilizing the principal of fluorescence resonance energy transfer (FRET), these novel structures were created by covalently linking a protein donor dye with an organic small molecule acceptor dye. Additionally, each of these fluorochrome conjugates were shown to be compatible with fixation/permeabilization buffer reagents, and demonstrated acceptable brightness and stability when conjugated to antigen‐specific monoclonal antibodies. These six novel fluorochrome reagents can increase the numbers of fluorochromes that can be used on a spectral flow cytometer. John Wiley & Sons, Inc. 2022-02-02 2022-10 /pmc/articles/PMC9790705/ /pubmed/35112484 http://dx.doi.org/10.1002/cyto.a.24537 Text en © 2022 AbbVie Inc. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Technical Note Seong, Yekyung Nguyen, Denny X Wu, Yian Thakur, Archana Harding, Fiona Nguyen, Tuan Andrew Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title | Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title_full | Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title_fullStr | Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title_full_unstemmed | Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title_short | Novel PE and APC tandems: Additional near‐infrared fluorochromes for use in spectral flow cytometry |
title_sort | novel pe and apc tandems: additional near‐infrared fluorochromes for use in spectral flow cytometry |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790705/ https://www.ncbi.nlm.nih.gov/pubmed/35112484 http://dx.doi.org/10.1002/cyto.a.24537 |
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