Publication:
Whole-mouse immunolabeling at cellular resolution for comprehensive 3D atlases

dc.contributor.coauthorMai, H.
dc.contributor.coauthorWang, Y.
dc.contributor.coauthorZhu, Y.
dc.contributor.coauthorZhao, Y.
dc.contributor.coauthorChen, Y.
dc.contributor.coauthorHoeher, L.
dc.contributor.coauthorAl-Maskari, R.
dc.contributor.coauthorLuo, J.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorErtürk, Ali Maximilian
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2026-07-07T08:50:44Z
dc.date.issued2026
dc.description.abstractThe wildDISCO protocol is used for whole-body immunolabeling, optical clearing and imaging of mice at cellular resolution using standard IgG antibodies. Mapping complex biological systems and tracking disease progression at high resolution across the entire mammalian body has remained technically challenging. Here, to address this, we present wildDISCO (immunolabeling of wild-type mice and DISCO clearing), a comprehensive protocol for whole-body immunolabeling, optical clearing and imaging of mice at cellular resolution using standard IgG antibodies. This protocol optimizes tissue permeabilization using cyclodextrin as a potent enhancer of cholesterol extraction and membrane permeabilization, enabling deep antibody penetration across all organs. We detail procedures for sample preparation, tissue decolorization and decalcification, whole-body immunostaining, clearing, and subsequent 3D imaging, virtual reality visualization and whole-mouse atlas construction. The method allows comprehensive mapping of neuronal, vascular, lymphatic and immune systems, as well as systemic studies in disease models, including cancer and microbiome–host interaction studies. We anticipate that wildDISCO will serve as a broadly applicable platform for generating whole-body cellular atlases, enabling systems-level investigations of health and disease. Only standard immunohistochemistry facilities are required, but successful implementation may require initial technical training, particularly for researchers with limited prior experience in tissue clearing or 3D imaging workflows. From start to finish, the procedure takes 4 weeks.
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipIllustrations (Fig. 1 and Supplementary Fig. 1) were created with BioRender.com.
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ1
dc.identifier.doi10.1038/s41596-026-01363-9
dc.identifier.eissn1750-2799
dc.identifier.embargoN/A
dc.identifier.endpage29
dc.identifier.issn1754-2189
dc.identifier.pubmed42045563
dc.identifier.scopus2-s2.0-105037317221
dc.identifier.startpage1
dc.identifier.urihttp://doi.org/10.1038/s41596-026-01363-9
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33361
dc.identifier.wos001750878100001
dc.keywordsImmunolabeling
dc.keywordsProtocol (science)
dc.keywordsVisualization
dc.keywordsHigh resolution
dc.keywordsLight sheet fluorescence microscopy
dc.keywordsResolution (logic)
dc.languageeng
dc.publisherNature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNature Protocols
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectBiochemistry
dc.subjectMolecular biology
dc.titleWhole-mouse immunolabeling at cellular resolution for comprehensive 3D atlases
dc.typeJournal Article
dspace.entity.typePublication
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