RRID:AB_2716551
DOI: 10.1016/j.ccell.2025.04.003
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1016/j.ccell.2025.04.003
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1016/j.celrep.2024.114003
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1016/j.immuni.2024.01.011
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1016/j.immuni.2024.01.011
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1016/j.isci.2024.108925
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
RRID:AB_2716551
DOI: 10.1038/s41467-021-27349-7
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
Curator: @scibot
SciCrunch record: RRID:AB_2716551
Immunohistochemistry was performed using a standard immunoperoxidase approach, as previously described [21]. To examine multiple antigens within the same FFPE section, samples were probed in a sequential manner with up to three different antibodies (ESM Tables 3, 4). The mean fluorescence intensity (MFI) of stained antigens was measured using ImageJ Version 1.50b Java 1.8.0_77; https://imagej.nih.gov/ij/download.html. Some slides were processed with isotype control antisera to confirm the specificity of labelling (ESM Fig. 1). Frozen sections were stained using a standard immunofluorescence approach [22].
(HLA, Ins, Glu, NLRC5, STAT1, B2M abs determined from supplementary)