recombinant human il 17f protein cf Search Results


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  • 93
    R&D Systems il 17f
    Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), <t>IL‐17F</t> (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P
    Il 17f, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/il 17f/product/R&D Systems
    Average 93 stars, based on 1 article reviews
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    il 17f - by Bioz Stars, 2021-09
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    95
    Thermo Fisher il 17f
    Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), <t>IL‐17F</t> (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P
    Il 17f, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/il 17f/product/Thermo Fisher
    Average 95 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    il 17f - by Bioz Stars, 2021-09
    95/100 stars
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    86
    Berkshire Corporation il 17f
    Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), <t>IL‐17F</t> (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P
    Il 17f, supplied by Berkshire Corporation, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/il 17f/product/Berkshire Corporation
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    il 17f - by Bioz Stars, 2021-09
    86/100 stars
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    94
    BioLegend il 17f
    Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), <t>IL‐17F</t> (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P
    Il 17f, supplied by BioLegend, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/il 17f/product/BioLegend
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    il 17f - by Bioz Stars, 2021-09
    94/100 stars
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    Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), IL‐17F (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P

    Journal: Experimental Dermatology

    Article Title: Development and characterization of a human Th17‐driven ex vivo skin inflammation model, et al. Development and characterization of a human Th17‐driven ex vivo skin inflammation model

    doi: 10.1111/exd.14160

    Figure Lengend Snippet: Characterization of cytokine release consecutive to Th17/Th1 activation. NativeSkin® models were either cultured under basal conditions or in the presence of the Th17 polarization cocktail (negative control), or injected with rhIL‐2, anti‐CD3/CD28 antibodies (in situ activation) in the absence (negative control) or presence of the Th17 polarization cocktail (InflammaSkin®) for 7 days. Protein levels of IL‐17A (A), IL‐17AF (B), IL‐17F (C), IL‐22 (D), IFN‐γ (E), TNF‐α (F), IL‐15 (G), IL‐10 (H), IL‐4 (I) and IL‐13 (J) were measured by ELISA (IL‐22) and MSD (all the other cytokines) in supernatant samples harvested after the last 24 h of 7 d of culture. Lowest limit of detection (LLOD) for each cytokine is indicated by a dotted line. Data are expressed as mean values ± SEM of pg/mL of secreted cytokines of models obtained from three different skin donors (n = 3). Two‐way ANOVA statistical analysis followed by Tukey's multiple comparison tests was used to compare protein levels. **** P

    Article Snippet: The lowest limit of detection (LLOD) was 0.1, 0.2, 4.1, 1.4, 3.67, 10, 0.4‐3.8, 2.3‐2.9, 0.1‐0.3 and 10‐25 pg/mL for IL‐4, IL‐10, IL‐13, IL‐15 IL‐17AF, IL‐17F, IL‐17A, IFN‐γ, TNF‐α and IL‐22, respectively.

    Techniques: Activation Assay, Cell Culture, Negative Control, Injection, In Situ, Enzyme-linked Immunosorbent Assay