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cytokine concentrations  (Proteintech)


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    Structured Review

    Proteintech cytokine concentrations
    Cytokine Concentrations, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytokine+concentrations/Human+CXCL10%2FIP-10+ELISA+Kit/pm41579801-61-2-37
    Average 94 stars, based on 20 article reviews
    cytokine concentrations - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Cinnamic Aldehyde Inhibits Lipopolysaccharide-Induced Chondrocyte Inflammation and Reduces Cartilage Degeneration by Blocking the Nuclear Factor-Kappa B Signaling Pathway.
    Article Snippet: .. Cytokine concentrations (IL 1b, IL 6, and TNF-a) were determined using a commercially available enzyme-linked immunosorbent assay (ELISA) kit in accordance with the manufacturer’s instructions (Proteintech Group Inc, Rosemont, IL, USA). ..

    Article Title: Propofol alleviates M1 polarization and neuroinflammation of microglia in a subarachnoid hemorrhage model in vitro , by targeting the miR-140-5p/TREM-1/NF-κB signaling axis.
    Article Snippet: .. Cytokine concentrations were measured by an IL-1β ELISA kit (KE10003; Proteintech, Rosemont, IL, USA), TNF-α ELISA kit (KE10002; Proteintech), and IL-6 ELISA kit (KE10008; Proteintech). .. Oxidative stress reaction analysis The BV-2 cells were collected and dissolved in 0.2% Triton X-100 (100-100 ML; Sigma-Aldrich, St. Louis, MO, USA).

    Article Title: Agmatine ameliorates poly(I:C)-induced lung injury through IL-10/STAT3-dependent reprogramming of macrophage inflammatory responses.
    Article Snippet: The emerging field of immunometabolism posits that endogenous metabolites are pivotal regulators of immune responses, yet their therapeutic exploitation remains nascent.. Investigating this paradigm in lung injury, we observed that agmatine, a decarboxylation product of L-arginine, was significantly depleted in poly(I:C)-induced murine lung injury and in a clinical cohort characterized by virus-associated pulmonary involvement, suggesting a potential association with lung pathology.. In mice, exogenous agmatine supplementation ameliorated lung pathology and weight loss, effects that were contingent upon reprogramming of macrophage inflammatory responses.

    Article Title: Nicotinamide mononucleotide attenuates airway epithelial barrier dysfunction via inhibiting SIRT3 SUMOylation in asthma.
    Article Snippet: Nicotinamide adenine dinucleotide (NAD) is an essential element in cellular metabolism that regulates fundamental biological processes.. Growing evidence suggests that a decline in NAD is a common pathological factor in various diseases and aging.. However, its role in airway epithelial barrier function in response to asthma remains underexplored.



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    Limited effects of itaconate and mesaconate on H7N7-induced inflammatory mediator production in lung and brain at 8 <t>dpi.</t> <t>Pro-inflammatory</t> <t>cytokine</t> levels were quantified by ELISA in lung (A–D) and brain (E–H) tissues from PBS-inoculated control and H7N7-infected mice treated with PBS, itaconate, or mesaconate at 8 dpi. (A–D) H7N7 infection induced robust pulmonary increases in IL-6 (B) , IL-1β (C) , and IFN-γ (D) , which were not attenuated by either metabolite treatment. (E–H) In the brain, H7N7 infection increased IL-6 (F) and IL-1β (G) levels, with itaconate treatment further enhancing TNF-α production (E) , whereas mesaconate treatment was associated with reduced IL-1β (G) and attenuated neuroinflammatory responses. Data are presented as mean ± SEM. Statistical analysis was performed using two-way ANOVA followed by Fisher’s LSD post hoc test (* p < 0.05, ** p < 0.01 and *** p < 0.001). Group sizes ranged from N = 3–5 mice per group.
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    Image Search Results


    Limited effects of itaconate and mesaconate on H7N7-induced inflammatory mediator production in lung and brain at 8 dpi. Pro-inflammatory cytokine levels were quantified by ELISA in lung (A–D) and brain (E–H) tissues from PBS-inoculated control and H7N7-infected mice treated with PBS, itaconate, or mesaconate at 8 dpi. (A–D) H7N7 infection induced robust pulmonary increases in IL-6 (B) , IL-1β (C) , and IFN-γ (D) , which were not attenuated by either metabolite treatment. (E–H) In the brain, H7N7 infection increased IL-6 (F) and IL-1β (G) levels, with itaconate treatment further enhancing TNF-α production (E) , whereas mesaconate treatment was associated with reduced IL-1β (G) and attenuated neuroinflammatory responses. Data are presented as mean ± SEM. Statistical analysis was performed using two-way ANOVA followed by Fisher’s LSD post hoc test (* p < 0.05, ** p < 0.01 and *** p < 0.001). Group sizes ranged from N = 3–5 mice per group.

    Journal: Frontiers in Immunology

    Article Title: Targeting neuroinflammation: itaconate and mesaconate as therapeutic strategies against H7N7 influenza-associated CNS damage

    doi: 10.3389/fimmu.2026.1776302

    Figure Lengend Snippet: Limited effects of itaconate and mesaconate on H7N7-induced inflammatory mediator production in lung and brain at 8 dpi. Pro-inflammatory cytokine levels were quantified by ELISA in lung (A–D) and brain (E–H) tissues from PBS-inoculated control and H7N7-infected mice treated with PBS, itaconate, or mesaconate at 8 dpi. (A–D) H7N7 infection induced robust pulmonary increases in IL-6 (B) , IL-1β (C) , and IFN-γ (D) , which were not attenuated by either metabolite treatment. (E–H) In the brain, H7N7 infection increased IL-6 (F) and IL-1β (G) levels, with itaconate treatment further enhancing TNF-α production (E) , whereas mesaconate treatment was associated with reduced IL-1β (G) and attenuated neuroinflammatory responses. Data are presented as mean ± SEM. Statistical analysis was performed using two-way ANOVA followed by Fisher’s LSD post hoc test (* p < 0.05, ** p < 0.01 and *** p < 0.001). Group sizes ranged from N = 3–5 mice per group.

    Article Snippet: Pro-inflammatory cytokine concentrations (TNF-α: Cat. # DY410, assay range: 31.2–2000 pg/mL; IL-6: Cat. # DY406, assay range: 15.6–1000 pg/mL; IL-1β: Cat. # DY401, assay range: 15.6–1000 pg/mL and IFN-γ: Cat. # DY485, assay range: 31.2–2000 pg/mL) were quantified using DuoSet ELISA kits (R&D Systems) according to the manufacturer’s instructions.

    Techniques: Enzyme-linked Immunosorbent Assay, Control, Infection

    Proposed model of immunometabolic modulation during neurotropic IAV infection. The schematic illustrates that following IAV infection, (1) pro-inflammatory cytokines released by activated peripheral monocytes and macrophages and/or viral particles themselves can access the brain and trigger neuroinflammatory responses. Whether in vivo treatment with itaconate or mesaconate directly inhibits viral replication remains unknown. (2) Mesaconate selectively reduced brain IL-1β and IL-6 levels, whereas itaconate (3) more robustly suppressed infection-induced microglial density and activation and attenuated (4) microglial morphological reactivity and synaptic remodeling associated with infection, (5) processes that are implicated in subsequent neurodegenerative changes. Collectively, the model supports emerging evidence that structurally related itaconate isomers engage partially overlapping yet mechanistically distinct signaling programs rather than differing solely in inhibitory potency ( Created in BioRender. https://BioRender.com/pqfhoem , is licensed under CC BY 4.0 ).

    Journal: Frontiers in Immunology

    Article Title: Targeting neuroinflammation: itaconate and mesaconate as therapeutic strategies against H7N7 influenza-associated CNS damage

    doi: 10.3389/fimmu.2026.1776302

    Figure Lengend Snippet: Proposed model of immunometabolic modulation during neurotropic IAV infection. The schematic illustrates that following IAV infection, (1) pro-inflammatory cytokines released by activated peripheral monocytes and macrophages and/or viral particles themselves can access the brain and trigger neuroinflammatory responses. Whether in vivo treatment with itaconate or mesaconate directly inhibits viral replication remains unknown. (2) Mesaconate selectively reduced brain IL-1β and IL-6 levels, whereas itaconate (3) more robustly suppressed infection-induced microglial density and activation and attenuated (4) microglial morphological reactivity and synaptic remodeling associated with infection, (5) processes that are implicated in subsequent neurodegenerative changes. Collectively, the model supports emerging evidence that structurally related itaconate isomers engage partially overlapping yet mechanistically distinct signaling programs rather than differing solely in inhibitory potency ( Created in BioRender. https://BioRender.com/pqfhoem , is licensed under CC BY 4.0 ).

    Article Snippet: Pro-inflammatory cytokine concentrations (TNF-α: Cat. # DY410, assay range: 31.2–2000 pg/mL; IL-6: Cat. # DY406, assay range: 15.6–1000 pg/mL; IL-1β: Cat. # DY401, assay range: 15.6–1000 pg/mL and IFN-γ: Cat. # DY485, assay range: 31.2–2000 pg/mL) were quantified using DuoSet ELISA kits (R&D Systems) according to the manufacturer’s instructions.

    Techniques: Infection, In Vivo, Activation Assay

    MSC NVs attenuated inflammation and their in vivo distribution. ( A ) Contents of the IL-1β, TNF-α, IFN-γ, IL-6, IL-12 p70, and IL-17A in the serum. ( B ) In vivo distribution of DIR-labeled MSC NVs. Fluorescent signals in the gastrointestinal tract, heart, liver, spleen, lungs, and kidneys of the mice at different time points. Means ± SD; * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: International Journal of Nanomedicine

    Article Title: Umbilical Cord Mesenchymal Stem Cell-Derived Extracellular Nanovesicles Alleviated Colitis via Modulating Th17/Treg Balance Through Hsa-miR-27b-3p-Mediated Suppression of PI3K/AKT/STAT3 Signaling Pathway

    doi: 10.2147/IJN.S565416

    Figure Lengend Snippet: MSC NVs attenuated inflammation and their in vivo distribution. ( A ) Contents of the IL-1β, TNF-α, IFN-γ, IL-6, IL-12 p70, and IL-17A in the serum. ( B ) In vivo distribution of DIR-labeled MSC NVs. Fluorescent signals in the gastrointestinal tract, heart, liver, spleen, lungs, and kidneys of the mice at different time points. Means ± SD; * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: Serum cytokine concentrations (IL-1β, TNF-α, IFN-γ, IL-6, IL-12 p70, and IL-17A) were quantified using commercial ELISA kits (Abclonal, Wuhan, China) according to the protocols.

    Techniques: In Vivo, Labeling