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Ab52587 nat105

Manufactured by Abcam
Sourced in United Kingdom

Ab52587/ NAT105 is a laboratory equipment product. It is designed for use in scientific research. The core function of this product is to provide a tool for researchers to conduct their experiments and studies.

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2 protocols using ab52587 nat105

1

Immunohistochemical Profiling of PD-1 and PD-L1

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Tissue microarrays (TMAs) had already been prepared for previous studies [4 (link), 25 (link)], by taking three cores of 0.6 mm from formalin-fixed paraffin-embedded (FFPE) tissue blocks. Of these blocks, 4-μm tissue sections were cut and then immunohistochemically stained for PD-1 and PD-L1 with the Ventana autostainer (Roche, Tuscon, AZ, USA), according to the instructions of the manufacturer. For PD-1, we used the mouse anti-PD-1 monoclonal antibody (ab52587/ NAT105, dilution 1:50; Abcam, Cambridge, UK) and for PD-L1, a rabbit anti-PD-L1 monoclonal antibody [741–4905 (clone sp263, dilution Ventana ready to use; Ventana Medical Systems, Tuscon, AZ, USA)]. ER (Ventana 1:100), PR (Dako 1:100), and HER2 (Neomarkers 1:100) were also stained with the Ventana autostainer.
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2

PD-L1 and PD-1 Expression Quantification

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Dual immunohistochemistry for PD-L1 and PD-1 expression was performed using Cell Signaling Technologies #13684 (clone E1L3N) and Abcam AB52587 (Nat105) in the Tissue Core Facility at Moffitt Cancer Center and evaluated on 37 cases total and 27/36 cases with evaluable responses to immunotherapy (Supplementary Fig. S2). PD-L1 expression was quantified using manual morphometric analysis in blinded fashion by a dermatopathologist (KYT). Given the large variability of tissue sample sizes, the following approach was used. PD-L1 expression was largely confined to the tumor periphery and quantitated on the basis of estimating the proportion of tumor cells expressing membranous or membranous and cytoplasmic PD-L1. The tumor periphery was defined here as the 50 micron-thick outer edge of every physically distinct tumor nodule. Within this region, the proportion of tumor cells exhibiting expression was quantitated as <1% (negative) or ≥1% (positive). All evaluated tumors had some expression of PD-L1.
Because of the relative paucity of PD-1 expression overall, the staining was scored solely on the basis of presence (1 (link)) or absence (0) of expression on peritumoral (within 0.02 mm = 20 microns of tumor periphery) lymphocytes (35 (link)).
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