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Department of Endocrinology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
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-rabbit IgG (H+L), Cat# 34206ES60) and Alexa Fluor 594 (donkey anti-mouse IgG (H+L), Cat# 34112ES60) were purchased from Yeasen Biotech Co (Shanghai, China). Cell culture, FFA preparation, and cell treatment MIN6 cells (passage 20–45) were routinely
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:1000,2438S, Cell Signaling Technology) primary antibodies. The membranes were incubated at room temperature for 1 h with the secondary antibodies (HRP-labeled goat anti-mouse IgG(H+L),1:1000, A0216, Beyotime; goat anti-rabbit IgG(H+L)-HRP antibody, 1
Department of Endocrinology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
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-risk autoantibodies and greatly improve sensitivity and disease specificity. Moreover, ECL assays, which capture all of the immunoglobulin classes (IgG, IgM, IgA, and IgE), are more sensitive than ELISA, which captures only IgG. More importantly, previous studies have
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, Abcam), NPHS2 (1:2000, ab181143, Abcam), GLP-1R (1:250, ab218532, Abcam), overnight at 4°C, HRP-labeled goat anti-rabbit secondary antibody immunoglobulin G (IgG) (1:50, A0208, Beyotime, Shanghai, China) was incubated at room temperature for 1 h, DAB
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overnight. Following washing, the sections were incubated with the horseradish peroxidase (HRP)-conjugated anti-rabbit IgG secondary antibody (cat. Ab6721, Abcam) at a dilution of 1:1000 for 1 h. The F4/80 signal was detected using the DAB method. Finally
Postgraduate Program in Nutritional Sciences, Department of Nutrition, Center for Health Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil
University Centre of João Pessoa (UNIPE), João Pessoa, Paraíba, Brazil
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Postgraduate Program in Cognitive Neuroscience and Behavior, Center for Health Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil
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Department of Biorregulation, Health Sciences Institute, Federal University of Bahia, Bahia, Brazil
Postgraduate Program in Medicine and Health, Medical School of Medicine, Federal University of Bahia, Salvador, Bahia, Brazil
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All patients tested positive for SARS-CoV-2 using the real-time quantitative reverse-transcriptase-PCR (rRT-qPCR) with samples from the respiratory tract and, in cases of negative rRT-qPCR, using clinical, radiological, and serological (IgG positive
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probed with secondary horseradish-peroxidase-conjugated IgG (1:10,000 dilution; Aspen, Wuhan, China) for 2 h at room temperature. The membranes were washed with ECL solution for 5 min and repeated for five times, followed by chemiluminescence detection in
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temperature. Primary GLP-1 antibodies (1:100, ab22625, Abcam) were diluted in the blocking solution, and the cells were incubated with the antibodies at room temperature for 2 h. Subsequently, Alexa Fluor 488 goat anti-mouse IgG (H&L) (1:1000, ab150113, Abcam