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14 protocols using sekm 0034

1

Quantifying Inflammatory Cytokines in BALF

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Levels of IL-1β, IL-6, IL-18, and TNF-α were measured in BALF using ELISA kits (cat. no. SEKM-0002, SEKM-0007, SEKM-0019, and SEKM-0034, Solarbio, Inc., China) according to manufacturer’s instructions. Optical density values were measured at 450 mm with a microplate reader (Varioskan LUX, ThermoFisher, USA) in each well.
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2

BV2 Microglia Cytokine ELISA

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Cell-free supernatants were collected from BV2 microglia cultures and analyzed for TNF-α (SEKM-0034, Solarbio, Beijing, China) and IL-6 (SEKM-0007, Solarbio) with ELISA kits, according to the manufacturer’s instructions.
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3

Cytokine Quantification Using ELISA

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Using ELISA kits (SEKM-0002, SEKM-0007, and SEKM-0034; Beijing Solarbio Science & Technology Co., Ltd., China), we measured the levels of IL-1, IL-6, and TNF- in the serum or culture supernatants. Testing was performed according to the manufacturer’s instructions.
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4

Modulation of LPS/LTA-induced Cytokine Production

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LPS and LTA (5 μg/mL) were each incubated with Crus2 or P58 (32 μM) or PBS (control) for 1 h at room temperature. J774.1 cells were cultured overnight in a 24-well plate (5 × 105 cells/well) and incubated with Crus2/P58-treated LPS/LTA or untreated LPS/LTA for 24 h at 37 °C. The culture supernatant was collected and used to measure IL-1β (EMC001b, Neobioscience, Shenzhen, China), IL-6 (SEKM0007, Solarbio, Beijing, China) and TNF-α (SEKM0034, Solarbio, Beijing, China) by ELISA according to the manufacturer’s instructions.
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5

Modulation of Cytokine Production by RNA-binding Proteins

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MEFs and mouse macrophages were seeded on a 24-well plate and transfected with DDX5, METTL3, and YTHDF2 using Lipofectamine 3000 DNA transfection reagents for 24 h, or with siDDX5, siMETTL3, siYTHDF2, and NC siRNA using Lipofectamine RNAi MAX transfection reagent for 48 h. Next, the cells were infected with P. multocida (multiplicity of infection [MoI] = 20), M. pneumoniae (MoI = 1000), and S. aureus (MoI = 20) for 4 h or they were treated with LPS, FSL-1, and Pam3CSK4 for 4 h. The supernatant from each culture was collected to measure the production of IL-6 using a mouse IL-6 enzyme-linked immunosorbent assay (ELISA) kit (SEKM-0007; Solarbio, Beijing, China) according to the manufacturer’s instructions. DDX5+/+ mice, DDX5+/- mice, Mettl3 cKO mice, and Mettl3 WT mice were infected with P. multocida (5 × 103 CFU/g) and S. aureus (5 × 105 CFU/g) for 6, or with M. pneumoniae (5 × 105 CFU/g) for 24 and 36 h. After that, mouse serum was collected to measure the production of IL-6 with the same ELISA kit as above. At the same time, mouse lungs were collected to measure the production of IL-6, as detailed above, and TNF-α using a mouse TNF-α ELISA kit (SEKM-0034; Solarbio, Beijing, China).
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6

Cytokine Profiling in Lung Tissues

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The levels of IL-6 (SEKM-0007 and SEKH-0013, Solarbio), tumor necrosis factor-α (TNF-α) (SEKM-0034 and SEKH-0047, Solarbio), IL-10 (SEKM-0010 and SEKH-0018, Solarbio), IL-18 (SEKH-0028 and SEKM-0019), and IL-1β (SEKM-0002 and SEKH-0002) in lung tissues and cell cultures were measured according to the instructions.
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7

Quantifying Cytokine Levels in Serum

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The concentrations of IL-1β (70-EK201B, MultiSciences, Hangzhou, China), IL-6 (RK00008, ABclonal), TNF-α (SEKM-0034, Solarbio, Beijing, China), and TGF-β1 (SEKM-0035, Solarbio) in the serum were measured using ELISA kits according to the manufacturers' instructions.
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8

Measurement of Inflammatory Biomarkers

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ELISA kits for the detection of Lp-PLA2 (CSB-E08321m, Cusabio, USA), TNF-α (SEKM-0034, Solarbio, China), IL-6 (SEKM-0007, Solarbio, China) and IL-1β (SEKM-0002, Solarbio, China) were obtained from Solarbio (Solarbio, Beijing, China). The levels of Lp-PLA2, TNF-α, IL-6 and IL-1β were analysed with corresponding ELISA kits according to the manufacturer's instructions. Then, the absorbance of the coloured product was measured at 405 nm by an automated plate reading system (FlexStation 3, Molecular Device, Sunnyvale, CA, USA). Each experiment was independently performed three times.
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9

Spinal Cord Cytokine Expression

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The protein expression of interleukin (il)-1β, tumor necrosis factor (TnF)-α and il-6 in lumbar dorsal spinal cord tissue homogenates were measured using commercially available eliSa kits (SEKM-0002, SEKM-0034 and SEKM-0007; Solarbio life Science), according to the manufacturer's protocols. The experiment was repeated three times, and the mean value was used.
Statistical analysis. SPSS (version 18.0; SPSS, inc.) was used for data analysis. data were presented as the mean ± standard deviation. comparisons between two groups were estimated by a Student's t-test, whereas multiple group comparisons were carried out by one-way anoVa analysis with a Bonferroni's post hoc test. P<0.05 was considered to indicate a statistically significant difference.
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10

Cytokine Profiling in Serum

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The levels of interleukin 6 (IL-6) (PI326; Beyotime, Beijing, China), tumor necrosis factor-α (TNF-α) (SEKM-0034, Solarbio), interleukin 1β (IL-1β) (SEKM-0002, Solarbio) in serum were detected using ELISA kits.
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