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Anti pd l1 monoclonal antibody clone e1l3n

Manufactured by Cell Signaling Technology
Sourced in United States

The Anti-PD-L1 monoclonal antibody (clone E1L3N) is a research-use only product manufactured by Cell Signaling Technology. It is designed to be used as a tool for the detection of PD-L1 protein expression in various biological samples.

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2 protocols using anti pd l1 monoclonal antibody clone e1l3n

1

mRNA and Protein Expression Analysis

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For mRNA expression, qRT-PCR analysis was performed using predefined TaqMan probes (Supplementary Data 1) chosen from the Thermo Fisher Scientific database (http://www.thermofisher.com). Using the High Capacity cDNA Reverse Transcription kit (Thermofisher), 1.5 µg of total RNA was reverse transcribed in a final volume of 50 µl. qPCR reactions were done using the high throughput BioMark HD system (Fluidigm) following manufacturer’s instructions. Pre-amplifications of 6 ng cDNA were performed using PreAmp Master Mix (Fluidigm) with a primer mix combining each primer used in the present study except the 18S probe due to it very high gene expression level. Expression data (Ct values) were acquired using the Fluidigm Real Time PCR Analysis software. The mean of 5 housekeeping genes (18S, ACTB, CLTC, GAPDH, and TBP) was used for the normalization of expression data. For protein expression, preparation of cells lysates from 30 frozen tumor samples and reverse phase protein array (RPPA) were performed as previously described42 (link). Array was revealed with the anti-PD-L1 monoclonal antibody (clone E1L3N; Cell Signaling Technology).
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2

NSCLC Immunotherapy Response Predictors

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Patients with advanced/recurrent/metastatic NSCLC treated with anti-PD-1 antibody (nivolumab or pembrolizumab) or anti-PD-L1 (atezolizumab) alone or in combination with chemotherapy at Kurume University Hospital (Kurume, Japan) or Kanagawa Cancer Center (Yokohama, Japan) were included in this study. Cohort 1, which included 123 patients enrolled between September 2016 and February 2020, was used as the training set for discovery; cohort 2, which included 99 patients enrolled between February 2020 and February 2021 and was completely independent from cohort 1, was used as the validation set. Patient characteristics are summarized in table 1. Tumor PD-L1 expression was determined by immunohistochemistry of paraffin-embedded tissue sections with an anti-PD-L1 monoclonal antibody (clone E1L3N; Cell Signaling Technology, Danvers, Massachusetts, USA; clone 22C3; Agilent Technologies/Dako, Carpinteria, California, USA). In most of the patients, PD-L1 expression was measured with tumor tissues obtained before the first-line treatment, even in those treated with ICI therapy as a second-line or later-line of treatment. The best clinical response was determined according to the Response Evaluation Criteria in Solid Tumors (RECIST) v.1.1.
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