Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/31835
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dc.contributor.authorPang, Lokman-
dc.contributor.authorErnst, Matthias-
dc.contributor.authorHuynh, Jennifer-
dc.date2022-12-
dc.date.accessioned2023-01-12T04:50:26Z-
dc.date.available2023-01-12T04:50:26Z-
dc.date.issued2023-
dc.identifier.citationMethods in Molecular Biology 2023en_US
dc.identifier.issn1940-6029-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/31835-
dc.description.abstractMultiplex immunohistochemistry (mIHC) facilitates the simultaneous detection of various immune cell markers on a single tissue section. Here, we describe a protocol for an mIHC staining workflow using specific antibodies against CD4, CD8α, FOXP3, and B220 to identify distinct lymphocyte populations including T and B cells. This staining strategy can be adapted to include other cell markers to evaluate the immune contexture in murine tissues.en_US
dc.language.isoeng-
dc.subjectCell surface markersen_US
dc.subjectImmune cellsen_US
dc.subjectMultiplex immunohistochemistryen_US
dc.subjectSpatial phenotypingen_US
dc.subjectTyramide signal amplification (TSA)en_US
dc.titleSpatially Characterizing the Immune Contexture in Mouse Tissue Using Multiplex Immunohistochemistry.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleMethods in Molecular Biologyen_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Instituteen_US
dc.identifier.doi10.1007/978-1-0716-2811-9_20en_US
dc.type.contentTexten_US
dc.identifier.pubmedid36513940-
dc.description.volume2593-
dc.description.startpage307-
dc.description.endpage316-
local.name.researcherErnst, Matthias
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
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