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Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo

We here report a flow-cytometry-based protocol to measure single-cell protein expression in small samples. The protocol is optimized for simultaneous detection of fluorescent proteins and intracellular and surface antigens in the embryonic pancreas from the mouse. Owing to low cell numbers, current...

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Detalles Bibliográficos
Autores principales: Nyeng, Pia, Dela Cruz, Gelo Victoriano, Semb, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255939/
https://www.ncbi.nlm.nih.gov/pubmed/34258596
http://dx.doi.org/10.1016/j.xpro.2021.100636
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author Nyeng, Pia
Dela Cruz, Gelo Victoriano
Semb, Henrik
author_facet Nyeng, Pia
Dela Cruz, Gelo Victoriano
Semb, Henrik
author_sort Nyeng, Pia
collection PubMed
description We here report a flow-cytometry-based protocol to measure single-cell protein expression in small samples. The protocol is optimized for simultaneous detection of fluorescent proteins and intracellular and surface antigens in the embryonic pancreas from the mouse. Owing to low cell numbers, current protocols for flow cytometric analysis of embryonic tissues rely on tissue pooling. Our protocol enables analysis of one pancreas per sample, thereby facilitating detection of biological variation and minimizing the number of experimental animals needed. For complete details on the use and execution of this protocol, please refer to Nyeng et al (2019).
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spelling pubmed-82559392021-07-12 Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo Nyeng, Pia Dela Cruz, Gelo Victoriano Semb, Henrik STAR Protoc Protocol We here report a flow-cytometry-based protocol to measure single-cell protein expression in small samples. The protocol is optimized for simultaneous detection of fluorescent proteins and intracellular and surface antigens in the embryonic pancreas from the mouse. Owing to low cell numbers, current protocols for flow cytometric analysis of embryonic tissues rely on tissue pooling. Our protocol enables analysis of one pancreas per sample, thereby facilitating detection of biological variation and minimizing the number of experimental animals needed. For complete details on the use and execution of this protocol, please refer to Nyeng et al (2019). Elsevier 2021-06-30 /pmc/articles/PMC8255939/ /pubmed/34258596 http://dx.doi.org/10.1016/j.xpro.2021.100636 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Nyeng, Pia
Dela Cruz, Gelo Victoriano
Semb, Henrik
Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title_full Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title_fullStr Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title_full_unstemmed Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title_short Flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
title_sort flow cytometry detection of surface and intracellular antigens in pancreas from a single mouse embryo
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255939/
https://www.ncbi.nlm.nih.gov/pubmed/34258596
http://dx.doi.org/10.1016/j.xpro.2021.100636
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