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il 13 duoset elisa  (R&D Systems)


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    R&D Systems il 13 duoset elisa
    Il 13 Duoset Elisa, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 41 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+il+13+duoset+elisa/Human+IL-13+DuoSet+ELISA/pm41858165-146-3-6
    Average 94 stars, based on 41 article reviews
    il 13 duoset elisa - by Bioz Stars, 2026-10
    94/100 stars

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    Enzyme-linked Immunosorbent Assay:

    Article Title: Differential Responsiveness of Human Skin Mast Cells to SCF and IL-33: Reduced Reactivity to SCF but Not to IL-33 in the Post-Mitotic Phase
    Article Snippet: .. ELISA assays were performed to quantify cytokine levels using the following kits, according to the manufacturers’ instructions: Human LIF ELISA Kit (Cat# BMS242, Thermo Fisher Scientific, Berlin, Germany), Human IL-13 DuoSet ELISA (Cat# DY213, R&D Systems, Wiesbaden, Germany), Human CCL1/I-309 DuoSet ELISA (Cat# DY272, R&D Systems), and Human TNF-α ELISA Kit (Cat# 88-7346-22, Thermo Fisher Scientific). .. Mast cells were washed twice in Ca 2+ /Mg 2+ free PBS, incubated with Zombie Violet (1:300, Biolegend, Koblenz, Germany) in PBS for 15 min and then blocked for 15 min at 4 °C with human AB-serum (Biotest, Dreieich, Germany) in FACS buffer (0.1% BSA, 0.5 mM EDTA).

    Article Title: Differential Responsiveness of Human Skin Mast Cells to SCF and IL-33: Reduced Reactivity to SCF but Not to IL-33 in the Post-Mitotic Phase
    Article Snippet: .. ELISA assays were performed to quantify cytokine levels using the following kits, according to the manufacturers’ instructions: Human LIF ELISA Kit (Cat# BMS242, Thermo Fisher Scientific, Berlin, Germany), Human IL-13 DuoSet ELISA (Cat# DY213, R&D Systems, Wiesbaden, Germany), Human CCL1/I-309 DuoSet ELISA https://doi.org/10.3390/cells15050398 (Cat# DY272, R&D Systems), and Human TNF-α ELISA Kit (Cat# 88-7346-22, Thermo Fisher Scientific). .. Mast cells were washed twice in Ca2+/Mg2+ free PBS, incubated with Zombie Violet (1:300, Biolegend, Koblenz, Germany) in PBS for 15 min and then blocked for 15 min at 4 ◦C with human AB-serum (Biotest, Dreieich, Germany) in FACS buffer (0.1% BSA, 0.5 mM EDTA).

    Article Title: Filaggrin insufficiency renders keratinocyte-derived small extracellular vesicles capable of affecting CD1a-mediated T cell responses and promoting allergic inflammation
    Article Snippet: IL-10 in cell culture supernatants was measured using the ELISA MAXTM Standard Set Human IL-10 (BioLegend) or Human IL-10 ELISA Set (Diaclone) according to manufacturer’s instructions using ELISA Coating Buffer (BioLegend). .. IL-13 in cell culture supernatants was measured using the Human IL-13 ELISA development kit (HRP) (Mabtech) or Human IL-13 DuoSet ELISA (R&D Systems) according to manufacturer’s instructions. .. For IL-17A measurement Human IL-17A ELISA development kit (HRP) (Mabtech) was used according to manufacturer’s instructions.

    Article Title: Keratinocyte-derived small extracellular vesicles supply antigens for CD1a-resticted T cells and promote their type 2 bias in the context of filaggrin insufficiency
    Article Snippet: IL-10 levels in cell culture supernatants were measured using the ELISA MAXTM Standard Set Human IL-10 (BioLegend) or Human IL-10 ELISA Set (Diaclone), according to the manufacturer’s instructions, using ELISA Coating Buffer (BioLegend). .. IL-13 in cell culture supernatants was measured using the Human IL-13 ELISA Development Kit (HRP) (Mabtech) or Human IL-13 DuoSet ELISA (R&D Systems) according to the manufacturer’s instructions. .. For IL-17A measurement Human IL-17A ELISA Development Kit (HRP) (Mabtech) was used, according to the manufacturer’s instructions.

    Cell Culture:

    Article Title: Filaggrin insufficiency renders keratinocyte-derived small extracellular vesicles capable of affecting CD1a-mediated T cell responses and promoting allergic inflammation
    Article Snippet: IL-10 in cell culture supernatants was measured using the ELISA MAXTM Standard Set Human IL-10 (BioLegend) or Human IL-10 ELISA Set (Diaclone) according to manufacturer’s instructions using ELISA Coating Buffer (BioLegend). .. IL-13 in cell culture supernatants was measured using the Human IL-13 ELISA development kit (HRP) (Mabtech) or Human IL-13 DuoSet ELISA (R&D Systems) according to manufacturer’s instructions. .. For IL-17A measurement Human IL-17A ELISA development kit (HRP) (Mabtech) was used according to manufacturer’s instructions.

    Article Title: Keratinocyte-derived small extracellular vesicles supply antigens for CD1a-resticted T cells and promote their type 2 bias in the context of filaggrin insufficiency
    Article Snippet: IL-10 levels in cell culture supernatants were measured using the ELISA MAXTM Standard Set Human IL-10 (BioLegend) or Human IL-10 ELISA Set (Diaclone), according to the manufacturer’s instructions, using ELISA Coating Buffer (BioLegend). .. IL-13 in cell culture supernatants was measured using the Human IL-13 ELISA Development Kit (HRP) (Mabtech) or Human IL-13 DuoSet ELISA (R&D Systems) according to the manufacturer’s instructions. .. For IL-17A measurement Human IL-17A ELISA Development Kit (HRP) (Mabtech) was used, according to the manufacturer’s instructions.



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    IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α <t>,</t> <t>IL-13</t> , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).
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    IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α <t>,</t> <t>IL-13</t> , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).
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    IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α <t>,</t> <t>IL-13</t> , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).
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    IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α <t>,</t> <t>IL-13</t> , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).
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    Image Search Results


    IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α , IL-13 , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).

    Journal: Cells

    Article Title: Differential Responsiveness of Human Skin Mast Cells to SCF and IL-33: Reduced Reactivity to SCF but Not to IL-33 in the Post-Mitotic Phase

    doi: 10.3390/cells15050398

    Figure Lengend Snippet: IL-33 and SCF differentially modulate cytokine production in skin MCs. ( a ) mRNA levels of CCL1 , TNF-α , IL-13 , and LIF were assessed by RT-qPCR following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized to three housekeeping genes ( ACTB , GAPDH , and PPIB ) and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants after stimulation. The data are presented as individual dots with mean ± SEM. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001; ns: not significant. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).

    Article Snippet: ELISA assays were performed to quantify cytokine levels using the following kits, according to the manufacturers’ instructions: Human LIF ELISA Kit (Cat# BMS242, Thermo Fisher Scientific, Berlin, Germany), Human IL-13 DuoSet ELISA (Cat# DY213, R&D Systems, Wiesbaden, Germany), Human CCL1/I-309 DuoSet ELISA (Cat# DY272, R&D Systems), and Human TNF-α ELISA Kit (Cat# 88-7346-22, Thermo Fisher Scientific).

    Techniques: Quantitative RT-PCR, Expressing, Control, Enzyme-linked Immunosorbent Assay, Software

    IL-33-induced cytokine responses tend to be more pronounced in post-mitotic cells, while SCF responsiveness remains broadly comparable between lifecycle phases. ( a ) mRNA levels of CCL1 , TNF-α , IL-13 and LIF were assessed by RT-qPCR in proliferative and post-mitotic MCs following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized as described in Methods and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants from proliferative and post-mitotic MCs. The data are presented as individual dots with mean ± SEM. * p < 0.05; **** p < 0.0001. pm indicates post-mitotic MCs; proli indicates proliferative MCs. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).

    Journal: Cells

    Article Title: Differential Responsiveness of Human Skin Mast Cells to SCF and IL-33: Reduced Reactivity to SCF but Not to IL-33 in the Post-Mitotic Phase

    doi: 10.3390/cells15050398

    Figure Lengend Snippet: IL-33-induced cytokine responses tend to be more pronounced in post-mitotic cells, while SCF responsiveness remains broadly comparable between lifecycle phases. ( a ) mRNA levels of CCL1 , TNF-α , IL-13 and LIF were assessed by RT-qPCR in proliferative and post-mitotic MCs following stimulation with IL-33 (green) or SCF (purple) for 90 min. Expression was normalized as described in Methods and is presented relative to the unstimulated control. ( b ) Protein concentrations of CCL1, TNF-α, IL-13, and LIF were determined by ELISA in culture supernatants from proliferative and post-mitotic MCs. The data are presented as individual dots with mean ± SEM. * p < 0.05; **** p < 0.0001. pm indicates post-mitotic MCs; proli indicates proliferative MCs. The figures were created using GraphPad Prism 10.4.2 (GraphPad Software, La Jolla, CA, USA, accessed on 23 February 2026).

    Article Snippet: ELISA assays were performed to quantify cytokine levels using the following kits, according to the manufacturers’ instructions: Human LIF ELISA Kit (Cat# BMS242, Thermo Fisher Scientific, Berlin, Germany), Human IL-13 DuoSet ELISA (Cat# DY213, R&D Systems, Wiesbaden, Germany), Human CCL1/I-309 DuoSet ELISA (Cat# DY272, R&D Systems), and Human TNF-α ELISA Kit (Cat# 88-7346-22, Thermo Fisher Scientific).

    Techniques: Quantitative RT-PCR, Expressing, Control, Enzyme-linked Immunosorbent Assay, Software