- Mar 2024
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www.sciencedirect.com www.sciencedirect.com
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RRID:AB_2716551
DOI: 10.1016/j.celrep.2024.114003
Resource: (Cell Signaling Technology Cat# 12851, RRID:AB_2716551)
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- Feb 2024
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www.sciencedirect.com www.sciencedirect.com
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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
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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
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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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
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- Dec 2021
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www.nature.com www.nature.com
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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
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- May 2020
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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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].
Immunohistochemistry
(HLA, Ins, Glu, NLRC5, STAT1, B2M abs determined from supplementary)
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