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5 protocols using bond epitope retrieval 1

1

Multiplex IHC for PD-L1 and CD8 Analysis

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Paraffin blocks of tumor tissues were sliced into 4 µm thick slides and heated at 60°C for 1 hour. The slides were dewaxed with xylene and stained with Leica Bond Rx Automated Stainer (Leica Biosystems). Afterwards, the slides were baked for 30 min, dewaxed, placed in Bond Epitope Retrieval 2 (Leica Biosystems) and Bond Epitope Retrieval 1 (Leica Biosystems) sequentially. The slides were incubated with the PD-L1 primary antibodies (13 684S) and CD8 (98 941S) and detected using the corresponding polymer horseradish peroxidase. Visualization was performed with using the Opal TSA Plus dye 690 and 720, respectively (Akoya Biosciences). Anti-CD8 antibody was incubated after incubation with the Opal TSA-DIG reagent (Perkin-Elmer). The nuclei were stained using DAPI (4′,6-diamidino-2-phenylindole) before the slides were covered using HIGHDEF IHC fluoromount (Enzo). The images were gained with PerkinElmer Vectra V.3.0 Automated Quantitative Pathology Imaging System (Perkin-Elmer) and evaluated with the InForm software V.2.2 and TIBCO Spotfire (Perkin-Elmer).
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2

Multispectral Fluorescence Staining Protocol

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Multispectral fluorescence staining was performed using the Opal 6-Plex Detection kit (Akoya Biosciences) using FFPE tissue sections. Slides were baked at 60°C for 15 minutes and deparaffinized with the Leica Bond Dewax solution (Leica Biosystems), followed by heat-based antigen retrieval using Bond Epitope Retrieval Solution 1 (Leica Biosystems) for 30 minutes. Using the Leica Bond Rx Automated Stainer (Leica Biosystems), slides were incubated with primary antibodies followed by the appropriate secondary horseradish peroxidase–conjugated polymer. Incubation was next performed with a unique Opal dye permitting fluorophore covalent bonding to the horseradish polymer. Heat-based retrieval with Bond Epitope Retrieval 1 (Leica Biosystems) was finally performed for 20 minutes. Slides were subjected to sequential rounds of staining. Primary antibodies, concentrations, and associated fluorophores are detailed in Supplemental Table 9. Sections were counterstained with Spectral DAPI and mounted with ProLong Diamond Antifade Mountant (Thermo Fisher Scientific). Images were acquired using the Vectra3 microscope (Akoya Biosciences) and Phenochart Whole Slide Viewer (Akoya Biosciences). Postacquisition image adjustments were performed using InForm Automated Image Analysis Software (Akoya Biosciences) and Fiji (74 (link)).
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Multiplex Fluorescence Staining for Tissue Analysis

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Multispectral fluorescence staining was performed using the Opal 6-Plex Detection kit (Akoya Biosciences, Marlborough, MA) using formalin-fixed, paraffin embedded tissue sections. Slides were baked at 60 °C for 15 min and deparaffinized with the Leica Bond Dewax solution (Leica Biosystems, Deer Park, IL), followed by heat-based antigen retrieval using Bond Epitope Retrieval Solution 1 (Leica Biosystems) for 30 min. Using the Leica Bond Rx Automated Stainer (Leica Biosystems), slides were incubated with primary antibodies followed by the appropriate secondary horseradish peroxidase-conjugated polymer. Incubation was next performed with a unique Opal dye permitting fluorophore covalent bonding to the horseradish polymer. Heat-based retrieval with Bond Epitope Retrieval 1 (Leica Biosystems) was finally performed for 20 min. Slides were subjected to sequential rounds of staining. Primary antibodies, concentrations, and associated fluorophores are detailed in Supplemental Table 9. Sections were counterstained with Spectral DAPI and mounted with ProLong Diamond Antifade Mountant (Thermo Fisher Scientific). Images were acquired using the Vectra3 microscope (Akoya Biosciences) and Phenochart Whole Slide Viewer (Akoya Biosciences). Post-acquisition image adjustments were performed using InForm Automated Image Analysis Software (Akoya Biosciences) and Fiji (76 (link)).
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4

Immunohistochemical Analysis of E-Cadherin and N-Cadherin

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Immunohistochemical stains were performed on 4-μm paraffin sections with the following primary antibodies: E-cadherin (clone 36, dilution 1:400; BD Transduction Laboratories, San Jose,CA, USA) and N-cadherin (clone 3B9, dilution 1:150;Invitrogen Life Technologies, Waltham, MA, USA). Immunohistochemical stains were performed using Leica Bond Automated stainer (Leica Biosystem, Buffalo Grove, IL, USA), Bond Epitope Retrieval 1 (Leica Biosystem), and Bond polymer Red refine detection kit (BD Biosciences, San Diego, CA, USA) according to the manufacturers' instructions. Omission of primary antibody was performed as a negative control. In addition, for N-cadherin, sections of myocardial tissue were used as a positive control and sections of bladder mucosa were used as a negative control. Normal skin epidermis was used as a positive control for E-cadherin immunostaining and dermis was used as a negative control. Pairing of tissue samples was blinded to the pathologists and slides of all immunohistochemical studies were reviewed by two independent dermatopathologists (SY and GS).
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5

Multispectral Fluorescence Staining Protocol

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Multispectral fluorescence staining was performed using the Opal 6-Plex Detection kit (Akoya Biosciences) using FFPE tissue sections. Slides were baked at 60°C for 15 minutes and deparaffinized with the Leica Bond Dewax solution (Leica Biosystems), followed by heat-based antigen retrieval using Bond Epitope Retrieval Solution 1 (Leica Biosystems) for 30 minutes. Using the Leica Bond Rx Automated Stainer (Leica Biosystems), slides were incubated with primary antibodies followed by the appropriate secondary horseradish peroxidase–conjugated polymer. Incubation was next performed with a unique Opal dye permitting fluorophore covalent bonding to the horseradish polymer. Heat-based retrieval with Bond Epitope Retrieval 1 (Leica Biosystems) was finally performed for 20 minutes. Slides were subjected to sequential rounds of staining. Primary antibodies, concentrations, and associated fluorophores are detailed in Supplemental Table 9. Sections were counterstained with Spectral DAPI and mounted with ProLong Diamond Antifade Mountant (Thermo Fisher Scientific). Images were acquired using the Vectra3 microscope (Akoya Biosciences) and Phenochart Whole Slide Viewer (Akoya Biosciences). Postacquisition image adjustments were performed using InForm Automated Image Analysis Software (Akoya Biosciences) and Fiji (74 (link)).
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