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Making Multiplexed Imaging Flexible: Combining Essential Markers With Established Antibody Panels
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science. A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.ORCID iD: 0000-0002-8200-6849
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science. KTH, Centres, Science for Life Laboratory, SciLifeLab.
KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Cellular and Clinical Proteomics.ORCID iD: 0000-0002-5375-459X
KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Cellular and Clinical Proteomics.ORCID iD: 0009-0003-6239-6952
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2024 (English)In: Journal of Histochemistry and Cytochemistry, ISSN 0022-1554, E-ISSN 1551-5044, Vol. 72, no 8-9, p. 517-544Article in journal (Refereed) Published
Abstract [en]

Multiplexed immunofluorescence (IF) can be achieved using different commercially available platforms, often making use of conjugated antibodies detected in iterative cycles. A growing portfolio of pre-conjugated antibodies is offered by the providers, as well as the possibility for in-house conjugation. For many conjugation methods and kits, there are limitations in which antibodies can be used, and conjugation results are sometimes irreproducible. The conjugation process can limit or slow down the progress of studies requiring conjugation of essential markers needed for a given project. Here, we demonstrate a protocol combining manual indirect immunofluorescence (IF) of primary antibodies, followed by antibody elution and staining with multiplexed panels of commercially pre-conjugated antibodies on the PhenoCycler platform. We present detailed protocols for applying the workflow on fresh frozen and formalin fixed paraffin embedded tissue sections. We also provide a ready to use workflow for coregistration of the images and demonstrate this for two examples.

Place, publisher, year, edition, pages
SAGE Publications , 2024. Vol. 72, no 8-9, p. 517-544
Keywords [en]
FFPE, fresh frozen, immunofluorescence, multiplexed imaging, PhenoCycler, spatial proteomics
National Category
Molecular Biology
Identifiers
URN: urn:nbn:se:kth:diva-366526DOI: 10.1369/00221554241274856ISI: 001303538100001PubMedID: 39215640Scopus ID: 2-s2.0-85203258736OAI: oai:DiVA.org:kth-366526DiVA, id: diva2:1982677
Note

QC 20250708

Available from: 2025-07-08 Created: 2025-07-08 Last updated: 2025-07-08Bibliographically approved

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Deen, Ashik JawaharThorsson, JohanO’Roberts, Eleanor M.Ullman, TonyOses, CarolinaStadler, Charlotte

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Deen, Ashik JawaharThorsson, JohanO’Roberts, Eleanor M.Panshikar, PranautiUllman, TonyOses, CarolinaStadler, Charlotte
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Protein ScienceScience for Life Laboratory, SciLifeLabCellular and Clinical Proteomics
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Journal of Histochemistry and Cytochemistry
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