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interleukin 5  (R&D Systems)


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    R&D Systems interleukin 5
    Interleukin 5, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/quantikine+human+il+5+elisa+kit/Human+IL-5+Quantikine+ELISA+Kit/pmc12932558-94-18-21
    Average 94 stars, based on 35 article reviews
    interleukin 5 - by Bioz Stars, 2026-09
    94/100 stars

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    Enzyme-linked Immunosorbent Assay:

    Article Title: Construction of SIV/HIV-1 chimeric viruses having the IL-5 gene and determination of their ability to replicate and produce IL-5.
    Article Snippet: During the progression of AIDS, there is a shift in abundance of immune cells from Th1-producing cells to Th2-producing cells.. To determine whether this change might have an effect on HIV-1 replication in vivo, we constructed simian/human immunodeficiency chimeric viruses having the human IL-5 gene (a Th2-type cytokine) and examined the effect of the inserted gene on viral replication, IL-5 production and viral stability in vitro.. The DNA of human IL-5 was inserted into vpr-deleted and nef-deleted infectious SHIVs.

    Article Title: New participant stratification and combination of urinary biomarkers and confounders could improve diagnostic accuracy for overactive bladder
    Article Snippet: .. The urinary (cell-free) concentrations of the candidate biomarkers were measured using ENLITEN® ATP Assay System Bioluminescence Detection Kit (FF2000, Promega, UK); Amplex® Red Acetylcholine/Acetylcholinesterase assay (InvitrogenTM Molecular ProbesTM, A12217, UK); Sievers Nitric Oxide Analyser (NOATM 280i, Analytix, UK); BD OptEIATM human MCP-1 enzyme-linked immunosorbent assay (ELISA) (559017, BD biosciences, UK); Quantikine® human IL-5 ELISA Kit (R&D Systems®, D5000B, UK) and the OptEIA TM Human IL-5 ELISA Set (555202, BD biosciences, UK) according to the manufacturers’ instructions. .. Urinary creatinine (Cr) was measured using the Cayman Creatinine (urinary) Colourimetric Assay Kit (CAY500701, Cambridge Bioscience, UK), following the manufacturer’s instructions.

    Article Title: Elevated levels of eotaxin and interleukin-5 in blister fluid of bullous pemphigoid: correlation with tissue eosinophilia.
    Article Snippet: Department of Dermatology, *Department of Allergy and Rheumatology, 2Department of Bioregulatory Function, Faculty of Medicine, University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan 3Department of Dermatology, Kanto Central Hospital, 6-25-1 Kamiyohga, Setagaya-ku, Tokyo 158-8531, Japan §Department of Dermatology, Kyushu University School of Medicine, 3-1-1 Maidashi Higashi-ku Fukuoka 812-8582, Fukuoka, Japan

    Article Title: An inflammatory stimulus sensitizes TRPA1 channel to increase cytokine release in human lung fibroblasts.
    Article Snippet: External stimuli such as cigarette smoke and house dust mite are often involved in the development and exacerbation of asthma.. These risk factors could activate or sensitize transient receptor potential channel ankyrin 1 (TRPA1), which are primarily expressed in neuronal structures but also in non-neuronal cells such as fibroblasts.. However, the role of non-neuronal TRPA1 in the pathophysiology of airway diseases including asthma remains unclear.

    ATP Assay:

    Article Title: New participant stratification and combination of urinary biomarkers and confounders could improve diagnostic accuracy for overactive bladder
    Article Snippet: .. The urinary (cell-free) concentrations of the candidate biomarkers were measured using ENLITEN® ATP Assay System Bioluminescence Detection Kit (FF2000, Promega, UK); Amplex® Red Acetylcholine/Acetylcholinesterase assay (InvitrogenTM Molecular ProbesTM, A12217, UK); Sievers Nitric Oxide Analyser (NOATM 280i, Analytix, UK); BD OptEIATM human MCP-1 enzyme-linked immunosorbent assay (ELISA) (559017, BD biosciences, UK); Quantikine® human IL-5 ELISA Kit (R&D Systems®, D5000B, UK) and the OptEIA TM Human IL-5 ELISA Set (555202, BD biosciences, UK) according to the manufacturers’ instructions. .. Urinary creatinine (Cr) was measured using the Cayman Creatinine (urinary) Colourimetric Assay Kit (CAY500701, Cambridge Bioscience, UK), following the manufacturer’s instructions.



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    Figure 1. CBD-X extract attenuates the differentiation and cytokine release of human T helper 2 (Th2) cells. CBD-X extract was added to isolated differentiated CD4 T cells. Then, Th2 cells were subjected to flow cytometry analysis. CBD-X-treated cells and their control cells were stained with human APC-CD4, BV421- CCR4 and FITC-CCR6. The means and standard deviations of the percentage of Th2 (CCR4+CCR6-) from CD4 population were calculated. (a) The means were calculated from three different experiments of ten healthy donors. Data were analyzed in comparison to differentiated DMSO treatment representative results for CBD-X-treated cells and their control cells are shown (b). Moreover, supernatants were collected and levels of pro-inflammatory cytokines IL5 (c) and IL-13 (d) were detected via <t>ELISA.</t> The means were calculated from healthy donors (black big dot); each dot represents one case. Data were normalized to differentiated cell groups and analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (* p < 0.05, *** p < 0.001).
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    Native and denatured LGI1 induce production and secretion of IL-10 in PBMCs from patients with LGI1 LE but not those from healthy controls. PBMCs of 4 patients with LGI1 LE (grey bars) and 10 healthy control volunteers (white bars) were incubated with native or denatured recombinant LGI1 or with cell culture medium and supernatant of non-transfected HEK 293 cells as vehicle controls. Cell culture supernatants were harvested after 4 days, and cytokine concentrations were determined with specific ELISA. <t>IFN-γ,</t> <t>IL-5,</t> IL-10, and IL-17 production are shown as means + SD; *** p < 0.001. Raw data are shown in .
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    R&D Systems human il 5 quantikine elisa kit r d systems cat
    Native and denatured LGI1 induce production and secretion of IL-10 in PBMCs from patients with LGI1 LE but not those from healthy controls. PBMCs of 4 patients with LGI1 LE (grey bars) and 10 healthy control volunteers (white bars) were incubated with native or denatured recombinant LGI1 or with cell culture medium and supernatant of non-transfected HEK 293 cells as vehicle controls. Cell culture supernatants were harvested after 4 days, and cytokine concentrations were determined with specific ELISA. <t>IFN-γ,</t> <t>IL-5,</t> IL-10, and IL-17 production are shown as means + SD; *** p < 0.001. Raw data are shown in .
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    Figure 1. CBD-X extract attenuates the differentiation and cytokine release of human T helper 2 (Th2) cells. CBD-X extract was added to isolated differentiated CD4 T cells. Then, Th2 cells were subjected to flow cytometry analysis. CBD-X-treated cells and their control cells were stained with human APC-CD4, BV421- CCR4 and FITC-CCR6. The means and standard deviations of the percentage of Th2 (CCR4+CCR6-) from CD4 population were calculated. (a) The means were calculated from three different experiments of ten healthy donors. Data were analyzed in comparison to differentiated DMSO treatment representative results for CBD-X-treated cells and their control cells are shown (b). Moreover, supernatants were collected and levels of pro-inflammatory cytokines IL5 (c) and IL-13 (d) were detected via ELISA. The means were calculated from healthy donors (black big dot); each dot represents one case. Data were normalized to differentiated cell groups and analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (* p < 0.05, *** p < 0.001).

    Journal: Pharmaceuticals (Basel, Switzerland)

    Article Title: High-CBD Extract (CBD-X) in Asthma Management: Reducing Th2-Driven Cytokine Secretion and Neutrophil/Eosinophil Activity.

    doi: 10.3390/ph17101382

    Figure Lengend Snippet: Figure 1. CBD-X extract attenuates the differentiation and cytokine release of human T helper 2 (Th2) cells. CBD-X extract was added to isolated differentiated CD4 T cells. Then, Th2 cells were subjected to flow cytometry analysis. CBD-X-treated cells and their control cells were stained with human APC-CD4, BV421- CCR4 and FITC-CCR6. The means and standard deviations of the percentage of Th2 (CCR4+CCR6-) from CD4 population were calculated. (a) The means were calculated from three different experiments of ten healthy donors. Data were analyzed in comparison to differentiated DMSO treatment representative results for CBD-X-treated cells and their control cells are shown (b). Moreover, supernatants were collected and levels of pro-inflammatory cytokines IL5 (c) and IL-13 (d) were detected via ELISA. The means were calculated from healthy donors (black big dot); each dot represents one case. Data were normalized to differentiated cell groups and analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (* p < 0.05, *** p < 0.001).

    Article Snippet: ELISA kits for human IL-5, IL-13, IL-8, and IL-6 or mouse IL-4, IL-5, and IL-13 were obtained from R&D System (Minneapolis, MN, USA).

    Techniques: Isolation, Flow Cytometry, Control, Staining, Comparison, Enzyme-linked Immunosorbent Assay

    Figure 2. CBD-X downregulates the secretion of pro-inflammatory cytokines from human neutrophils. Isolated neutrophils were treated with 2 µg/mL CBD-X. Treated cells were activated via 100 ng/mL LPS overnight. Levels of IL-8 and IL-6 (a,b) were detected via ELISA. Each colored dot represents one donor. The means were calculated from healthy donors (black big dot) and each dot represents one case. Data were analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (** p < 0.01, *** p < 0.001).

    Journal: Pharmaceuticals (Basel, Switzerland)

    Article Title: High-CBD Extract (CBD-X) in Asthma Management: Reducing Th2-Driven Cytokine Secretion and Neutrophil/Eosinophil Activity.

    doi: 10.3390/ph17101382

    Figure Lengend Snippet: Figure 2. CBD-X downregulates the secretion of pro-inflammatory cytokines from human neutrophils. Isolated neutrophils were treated with 2 µg/mL CBD-X. Treated cells were activated via 100 ng/mL LPS overnight. Levels of IL-8 and IL-6 (a,b) were detected via ELISA. Each colored dot represents one donor. The means were calculated from healthy donors (black big dot) and each dot represents one case. Data were analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (** p < 0.01, *** p < 0.001).

    Article Snippet: ELISA kits for human IL-5, IL-13, IL-8, and IL-6 or mouse IL-4, IL-5, and IL-13 were obtained from R&D System (Minneapolis, MN, USA).

    Techniques: Isolation, Enzyme-linked Immunosorbent Assay

    Figure 4. CBD-X extract attenuates serum OVA- IgE and BALF cytokine levels in an asthma mouse model. BALB/c mice were induced with OVA and were treated with 150 mg/kg CBD-X extract. Mice were euthanized, blood and lung fluids were collected. Levels of serum OVA- IgE (a) were detected via ELISA. Alternatively, levels of the pro-inflammatory IL-4 (b), IL-5 (c), and IL-13 (d) were also detected in the lung fluids via ELISA. Each colored dot represents one mouse. Standard deviations were calculated as the means of three biologically independent experiments (black big dot); n = 10. Data were analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (* p <0.05, ** p < 0.01, *** p < 0.001).

    Journal: Pharmaceuticals (Basel, Switzerland)

    Article Title: High-CBD Extract (CBD-X) in Asthma Management: Reducing Th2-Driven Cytokine Secretion and Neutrophil/Eosinophil Activity.

    doi: 10.3390/ph17101382

    Figure Lengend Snippet: Figure 4. CBD-X extract attenuates serum OVA- IgE and BALF cytokine levels in an asthma mouse model. BALB/c mice were induced with OVA and were treated with 150 mg/kg CBD-X extract. Mice were euthanized, blood and lung fluids were collected. Levels of serum OVA- IgE (a) were detected via ELISA. Alternatively, levels of the pro-inflammatory IL-4 (b), IL-5 (c), and IL-13 (d) were also detected in the lung fluids via ELISA. Each colored dot represents one mouse. Standard deviations were calculated as the means of three biologically independent experiments (black big dot); n = 10. Data were analyzed via one-way ANOVA (Fisher’s LSD test with values p < 0.05 considered statistically significant, (* p <0.05, ** p < 0.01, *** p < 0.001).

    Article Snippet: ELISA kits for human IL-5, IL-13, IL-8, and IL-6 or mouse IL-4, IL-5, and IL-13 were obtained from R&D System (Minneapolis, MN, USA).

    Techniques: Enzyme-linked Immunosorbent Assay

    Native and denatured LGI1 induce production and secretion of IL-10 in PBMCs from patients with LGI1 LE but not those from healthy controls. PBMCs of 4 patients with LGI1 LE (grey bars) and 10 healthy control volunteers (white bars) were incubated with native or denatured recombinant LGI1 or with cell culture medium and supernatant of non-transfected HEK 293 cells as vehicle controls. Cell culture supernatants were harvested after 4 days, and cytokine concentrations were determined with specific ELISA. IFN-γ, IL-5, IL-10, and IL-17 production are shown as means + SD; *** p < 0.001. Raw data are shown in .

    Journal: International Journal of Molecular Sciences

    Article Title: Leucine-Rich Glioma-Inactivated 1 (LGI1) Protein Stimulates Proliferation and IL-10 Production in Peripheral Blood Mononuclear Cells of Patients with LGI1 Antibody-Mediated Autoimmune Encephalitis In Vitro

    doi: 10.3390/ijms25052581

    Figure Lengend Snippet: Native and denatured LGI1 induce production and secretion of IL-10 in PBMCs from patients with LGI1 LE but not those from healthy controls. PBMCs of 4 patients with LGI1 LE (grey bars) and 10 healthy control volunteers (white bars) were incubated with native or denatured recombinant LGI1 or with cell culture medium and supernatant of non-transfected HEK 293 cells as vehicle controls. Cell culture supernatants were harvested after 4 days, and cytokine concentrations were determined with specific ELISA. IFN-γ, IL-5, IL-10, and IL-17 production are shown as means + SD; *** p < 0.001. Raw data are shown in .

    Article Snippet: The concentrations of IFN-γ (#DIF50C), IL-5 (#D5000B), IL-10 (#D1000B), and IL-17 (#D1700) in these cell culture supernatants were determined using specific ELISA systems (bio-techne, R&D Systems, Minneapolis, MN, USA) according to the manufacturer’s instructions.

    Techniques: Incubation, Recombinant, Cell Culture, Transfection, Enzyme-linked Immunosorbent Assay