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dc.contributor.authorAlejandre, Alba Méndez-
dc.date.accessioned2023-11-12T03:47:36Z-
dc.date.available2023-11-12T03:47:36Z-
dc.date.issued2023-
dc.identifier.otherOER000002542vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/23406-
dc.description.abstractPhagosome acidification and proteolysis are essential processes in the immune response to contain and eliminate pathogens. In recent years, there has been an increased desire for a rapid and accurate method of assessing these processes in real-time. Here, we outline the development of a multiplexed assay that allows simultaneous monitoring of phagosome acidification and proteolysis in the same sample using silica beads conjugated to pHrodo and DQ BSA. We describe in detail how to prepare the bi-functional particles and show proof of concept using differentially activated macrophages. This multiplexed spectrophotometric assay allows rapid and accurate assessment of phagosome acidification and proteolysis in real-time and could provide valuable information for understanding the immune response to pathogen invasionvi
dc.description.urihttps://www.biorxiv.org/content/10.1101/2023.04.03.535364v1.full.pdf+htmlvi
dc.formatPDFvi
dc.language.isoenvi
dc.publisherBioRxivvi
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Vietnam*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/vn/*
dc.subjectaxit hóavi
dc.subjectproteinvi
dc.subjectđại thực bàovi
dc.subjectxét nghiệmvi
dc.subject.lccTP359vi
dc.titleBi-functional particles for real-time acidification and proteolysis multiplex assay in macrophagesvi
dc.typeIndustry articlevi
dc.description.noteCC BY 4.0vi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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