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human total il 18  (R&D Systems)


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    Structured Review

    R&D Systems human total il 18
    Human Total Il 18, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 215 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+total+il+18+duoset+elisa/Human+Total+IL-18+DuoSet+ELISA/10__1158_slash_2326___6066__cir___25___1399-112-11-26
    Average 96 stars, based on 215 article reviews
    human total il 18 - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Gasdermin-D pores induce an inactivating caspase-4 cleavage that limits IL-18 production in the intestinal epithelium.
    Article Snippet: .. IL-18 was measured using Human Total IL-18 DuoSet ELISA (R&D Systems) as per manufacturer’s instructions. qPCR Cell pellets were washed in PBS. .. Total RNA was isolated using GeneJET RNA purification kit (Thermo Fisher).

    Article Title: Gasdermin-D pores induce an inactivating caspase-4 cleavage that limits IL-18 production in the intestinal epithelium
    Article Snippet: .. IL-18 was measured using Human Total IL-18 DuoSet ELISA (R&D Systems) as per manufacturer’s instructions. ..

    Article Title: ECDD-S16, a synthetic derivative of cleistanthin A, suppresses pyroptosis in Burkholderia pseudomallei- infected U937 macrophages
    Article Snippet: .. Cytokine production levels were measured by using Human IL-1β DuoSet ELISA, Human Total IL-18 DuoSet ELISA, Human IL-10 DuoSet ELISA (R&D Systems) and Human TNF ELISA Set (BD Biosciences) following the manufacturer’s instructions. .. Briefly, U937 monocyte-like cells (1.75 × 10 4 cells/well) were seeded onto a flat-bottom 96-well plate (Corning) and differentiated into macrophage-like cells as described above in cell line and culture condition.

    Article Title: BACH2 promotes seeding and establishment of long-lived HIV-1 reservoir in memory CD4 + T cells
    Article Snippet: .. In addition, IL-18 concentration was determined using the Human Total IL-18 DuoSet ELISA (R&D Systems). ..

    Article Title: Anti-oxidant and anti-inflammatory Effects of Aerosolised microalgal-derived extracellular vesicles in Bronchial Epithelial–Macrophage Co-cultures at the Air-Liquid Interface
    Article Snippet: .. The levels of the pro-inflammatory cytokine IL-8 and IL-18 were measured using the Human IL-8/CXCL8 DuoSet ELISA Kit (R&D Systems, DY208) and Human Total IL-18 DuoSet ELISA (R&D Systems, DY318) following the manufacturer’s recommendations. ..

    Article Title: ECDD-S16, a synthetic derivative of cleistanthin A, suppresses pyroptosis in Burkholderia pseudomallei-infected U937 macrophages.
    Article Snippet: .. Cytokine production levels were measured by using Human IL-1β DuoSet ELISA, Human Total IL-18 DuoSet ELISA, Human IL-10 DuoSet ELISA (R&D Systems) and Human TNF ELISA Set (BD Biosciences) following the manufacturer’s instructions. .. Briefly, U937 monocyte-like cells (1.75 × 104 cells/well) were seeded onto a flat-bottom 96-well plate (Corning) and differentiated into macrophage-like cells as described above in cell line and culture condition.

    Article Title: BACH2 promotes seeding and establishment of long-lived HIV-1 reservoir in memory CD4 + T cells.
    Article Snippet: .. In addition, IL-18 concentration was determined using the Human Total IL-18 DuoSet ELISA (R&D Systems). ..

    Article Title: Putative α7-selective ligands interact with α9-containing nicotinic acetylcholine receptors and modulate immune functions of human mononuclear phagocytes
    Article Snippet: Detached cells were then seeded in FBS-free RPMI 1640 medium in a density of 0.05 x 10 6 cells in 96-well plates (Greiner). .. Cytokine concentrations of IL-1β and IL-18 were measured in the above-described cell-free supernatants using the human IL-1 beta/IL-1F2 DuoSet enzyme-linked immunosorbent assay (ELISA) from R&D Systems (Cat# DY201) and human Total IL-18 DuoSet ELISA (Cat# DY318-05) according to the supplier’s instructions. .. Cytokine concentrations of IL-1β and IL-18 were measured in the above-described cell-free supernatants using the human IL-1 beta/IL-1F2 DuoSet enzyme-linked immunosorbent assay (ELISA) from R&D Systems (Cat# DY201) and human Total IL-18 DuoSet ELISA (Cat# DY318-05) according to the supplier’s instructions.

    Real-time Polymerase Chain Reaction:

    Article Title: Gasdermin-D pores induce an inactivating caspase-4 cleavage that limits IL-18 production in the intestinal epithelium.
    Article Snippet: .. IL-18 was measured using Human Total IL-18 DuoSet ELISA (R&D Systems) as per manufacturer’s instructions. qPCR Cell pellets were washed in PBS. .. Total RNA was isolated using GeneJET RNA purification kit (Thermo Fisher).

    Concentration Assay:

    Article Title: BACH2 promotes seeding and establishment of long-lived HIV-1 reservoir in memory CD4 + T cells
    Article Snippet: .. In addition, IL-18 concentration was determined using the Human Total IL-18 DuoSet ELISA (R&D Systems). ..

    Article Title: BACH2 promotes seeding and establishment of long-lived HIV-1 reservoir in memory CD4 + T cells.
    Article Snippet: .. In addition, IL-18 concentration was determined using the Human Total IL-18 DuoSet ELISA (R&D Systems). ..



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    Cytokine secretion profile of CALU-3/dTHP-1 coculture following exposure to nebulized LPS. ( A ) IL-6, ( B ) IL-8, ( C ) IL-1β, ( D ) <t>IL-18,</t> (E) TNF-α, and ( F ) IL-10 were quantified after exposure to 125 and 250 µg/mL nebulized LPS solution for 24 hours. Data are presented as mean ± SEM from three independent experiments. Statistical significance was determined using one-way ANOVA (*p< 0.5, **p < 0.01).
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    (A) Schematic representation of the cell treatment protocol. For the Doxorubicin-treated (Doxo) samples (blue), cells were seeded at day -3, and Doxo was added at day 0 for 24h. For the control samples (green), cells were seeded at day 0, and treated with DMSO for 24h at day 3. For both conditions, the senescent assays were performed at day 7 after treatment. (B) Proliferation assay at day 7 following 24h Doxo treatment across doses from 65–1000 nM. Ratios represent cell number at day 7 relative to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of IL-6 <t>and</t> <t>IL-8</t> secretion at day 7 (mean ± SD). Statistical analysis: Mann-Whitney t-test; N = 2, n = 3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.
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    (A) Schematic representation of the cell treatment protocol. For the Doxorubicin-treated (Doxo) samples (blue), cells were seeded at day -3, and Doxo was added at day 0 for 24h. For the control samples (green), cells were seeded at day 0, and treated with DMSO for 24h at day 3. For both conditions, the senescent assays were performed at day 7 after treatment. (B) Proliferation assay at day 7 following 24h Doxo treatment across doses from 65–1000 nM. Ratios represent cell number at day 7 relative to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of IL-6 <t>and</t> <t>IL-8</t> secretion at day 7 (mean ± SD). Statistical analysis: Mann-Whitney t-test; N = 2, n = 3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.
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    (A) Schematic representation of the cell treatment protocol. For the Doxorubicin-treated (Doxo) samples (blue), cells were seeded at day -3, and Doxo was added at day 0 for 24h. For the control samples (green), cells were seeded at day 0, and treated with DMSO for 24h at day 3. For both conditions, the senescent assays were performed at day 7 after treatment. (B) Proliferation assay at day 7 following 24h Doxo treatment across doses from 65–1000 nM. Ratios represent cell number at day 7 relative to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of IL-6 <t>and</t> <t>IL-8</t> secretion at day 7 (mean ± SD). Statistical analysis: Mann-Whitney t-test; N = 2, n = 3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.
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    Image Search Results


    Cytokine secretion profile of CALU-3/dTHP-1 coculture following exposure to nebulized LPS. ( A ) IL-6, ( B ) IL-8, ( C ) IL-1β, ( D ) IL-18, (E) TNF-α, and ( F ) IL-10 were quantified after exposure to 125 and 250 µg/mL nebulized LPS solution for 24 hours. Data are presented as mean ± SEM from three independent experiments. Statistical significance was determined using one-way ANOVA (*p< 0.5, **p < 0.01).

    Journal: bioRxiv

    Article Title: Anti-oxidant and anti-inflammatory Effects of Aerosolised microalgal-derived extracellular vesicles in Bronchial Epithelial–Macrophage Co-cultures at the Air-Liquid Interface

    doi: 10.64898/2026.03.19.712886

    Figure Lengend Snippet: Cytokine secretion profile of CALU-3/dTHP-1 coculture following exposure to nebulized LPS. ( A ) IL-6, ( B ) IL-8, ( C ) IL-1β, ( D ) IL-18, (E) TNF-α, and ( F ) IL-10 were quantified after exposure to 125 and 250 µg/mL nebulized LPS solution for 24 hours. Data are presented as mean ± SEM from three independent experiments. Statistical significance was determined using one-way ANOVA (*p< 0.5, **p < 0.01).

    Article Snippet: The levels of the pro-inflammatory cytokine IL-8 and IL-18 were measured using the Human IL-8/CXCL8 DuoSet ELISA Kit (R&D Systems, DY208) and Human Total IL-18 DuoSet ELISA (R&D Systems, DY318) following the manufacturer’s recommendations.

    Techniques:

    (A) Schematic representation of the cell treatment protocol. For the Doxorubicin-treated (Doxo) samples (blue), cells were seeded at day -3, and Doxo was added at day 0 for 24h. For the control samples (green), cells were seeded at day 0, and treated with DMSO for 24h at day 3. For both conditions, the senescent assays were performed at day 7 after treatment. (B) Proliferation assay at day 7 following 24h Doxo treatment across doses from 65–1000 nM. Ratios represent cell number at day 7 relative to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of IL-6 and IL-8 secretion at day 7 (mean ± SD). Statistical analysis: Mann-Whitney t-test; N = 2, n = 3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.

    Journal: bioRxiv

    Article Title: Stiffness Drives Endothelial Senescence and Inflammation in Aging and Doxorubicin-Induced Vascular Dysfunction

    doi: 10.64898/2026.01.30.702284

    Figure Lengend Snippet: (A) Schematic representation of the cell treatment protocol. For the Doxorubicin-treated (Doxo) samples (blue), cells were seeded at day -3, and Doxo was added at day 0 for 24h. For the control samples (green), cells were seeded at day 0, and treated with DMSO for 24h at day 3. For both conditions, the senescent assays were performed at day 7 after treatment. (B) Proliferation assay at day 7 following 24h Doxo treatment across doses from 65–1000 nM. Ratios represent cell number at day 7 relative to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of IL-6 and IL-8 secretion at day 7 (mean ± SD). Statistical analysis: Mann-Whitney t-test; N = 2, n = 3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.

    Article Snippet: Human IL-6 and IL-8 DuoSet ELISA kits (R&D Systems) were used according to the manufacturer’s instructions.

    Techniques: Control, Proliferation Assay, Staining, Immunofluorescence, Enzyme-linked Immunosorbent Assay, MANN-WHITNEY

    (A) Schematic representation of the protocol followed to obtain replicative senescence (RS). (B) Growth rate assessed as the ratio of cell number at day 7 to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of secreted IL-6 and IL-8 in RS cells versus controls. Statistical analysis: Mann–Whitney t-test. N=2–3, n=3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.

    Journal: bioRxiv

    Article Title: Stiffness Drives Endothelial Senescence and Inflammation in Aging and Doxorubicin-Induced Vascular Dysfunction

    doi: 10.64898/2026.01.30.702284

    Figure Lengend Snippet: (A) Schematic representation of the protocol followed to obtain replicative senescence (RS). (B) Growth rate assessed as the ratio of cell number at day 7 to day 0 (mean ± SD). (C) Left: representative bright-field images of the β -Galactosidase ( β -Gal) staining at day 7, scale bar 100 µ m. Right: Representative immunofluorescence images: γ -H2AX (magenta), nuclei (blue); scale bar 20 µ m. (D) β -Gal positivity at day 7 (mean ± SD). (E) DNA damage measured by γ -H2AX foci per nucleus (mean ± SEM). (F) ELISA quantification of secreted IL-6 and IL-8 in RS cells versus controls. Statistical analysis: Mann–Whitney t-test. N=2–3, n=3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001.

    Article Snippet: Human IL-6 and IL-8 DuoSet ELISA kits (R&D Systems) were used according to the manufacturer’s instructions.

    Techniques: Staining, Immunofluorescence, Enzyme-linked Immunosorbent Assay, MANN-WHITNEY

    A) IL-6 and IL-8 secretion levels in control, Doxotreated, and RS populations after 7 days, quantified by ELISA and normalized to cell number (mean ± SEM). Statistical analysis: two-way ANOVA with Tukey’s post hoc test (ELISA), N=3, n=3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001. B) Gene Ontology (GO) enrichment analysis displaying the top 10 Biological Process (BP) terms with highest statistical significance for Control vs Doxo and Control vs RS comparisons, respectively. For all GO term graphs, vertical axis shows GO terms and horizontal axis shows GeneRatio which corresponds to the genes of interest in the sample gene set divided over the total number of genes in the GO term. The size of each term dot represents the total count of genes identified in the sample gene set belonging to the term and the colour describes statistical significance according to the p-adjust legend. Recurring terms include chemotaxis, leukocyte migration, and extracellular matrix organization. Statistical analysis: DESeq2 (RNA-seq). N=3, n=3.

    Journal: bioRxiv

    Article Title: Stiffness Drives Endothelial Senescence and Inflammation in Aging and Doxorubicin-Induced Vascular Dysfunction

    doi: 10.64898/2026.01.30.702284

    Figure Lengend Snippet: A) IL-6 and IL-8 secretion levels in control, Doxotreated, and RS populations after 7 days, quantified by ELISA and normalized to cell number (mean ± SEM). Statistical analysis: two-way ANOVA with Tukey’s post hoc test (ELISA), N=3, n=3. Significance: * ≤ 0.05, ** ≤ 0.01, *** ≤ 0.001, **** ≤ 0.0001. B) Gene Ontology (GO) enrichment analysis displaying the top 10 Biological Process (BP) terms with highest statistical significance for Control vs Doxo and Control vs RS comparisons, respectively. For all GO term graphs, vertical axis shows GO terms and horizontal axis shows GeneRatio which corresponds to the genes of interest in the sample gene set divided over the total number of genes in the GO term. The size of each term dot represents the total count of genes identified in the sample gene set belonging to the term and the colour describes statistical significance according to the p-adjust legend. Recurring terms include chemotaxis, leukocyte migration, and extracellular matrix organization. Statistical analysis: DESeq2 (RNA-seq). N=3, n=3.

    Article Snippet: Human IL-6 and IL-8 DuoSet ELISA kits (R&D Systems) were used according to the manufacturer’s instructions.

    Techniques: Control, Enzyme-linked Immunosorbent Assay, Chemotaxis Assay, Migration, RNA Sequencing