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thp 1 dualtm reporter cells  (InvivoGen)


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    Structured Review

    InvivoGen thp 1 dualtm reporter cells
    Modulation of NF-κB and IRF signaling pathways <t>in</t> <t>THP-1</t> Dual cells by LL-37 and Polymyxin B. (A) NF-κB activity quantified using the Quanti-Blue assay. (B) IRF activity measured using the Quanti-Luc assay. Data represent mean ± SD. Statistical significance relative to the untreated condition was determined using a paired t -test with Benjamini-Hochberg correction for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
    Thp 1 Dualtm Reporter Cells, supplied by InvivoGen, used in various techniques. Bioz Stars score: 96/100, based on 517 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/thp 1 dualtm reporter cells/product/InvivoGen
    Average 96 stars, based on 517 article reviews
    thp 1 dualtm reporter cells - by Bioz Stars, 2026-06
    96/100 stars

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    1) Product Images from "Modulation of LPS-associated virulence activity for reduction of periodontal inflammatory burden"

    Article Title: Modulation of LPS-associated virulence activity for reduction of periodontal inflammatory burden

    Journal: Frontiers in Microbiology

    doi: 10.3389/fmicb.2026.1728315

    Modulation of NF-κB and IRF signaling pathways in THP-1 Dual cells by LL-37 and Polymyxin B. (A) NF-κB activity quantified using the Quanti-Blue assay. (B) IRF activity measured using the Quanti-Luc assay. Data represent mean ± SD. Statistical significance relative to the untreated condition was determined using a paired t -test with Benjamini-Hochberg correction for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
    Figure Legend Snippet: Modulation of NF-κB and IRF signaling pathways in THP-1 Dual cells by LL-37 and Polymyxin B. (A) NF-κB activity quantified using the Quanti-Blue assay. (B) IRF activity measured using the Quanti-Luc assay. Data represent mean ± SD. Statistical significance relative to the untreated condition was determined using a paired t -test with Benjamini-Hochberg correction for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Techniques Used: Protein-Protein interactions, Activity Assay

    Cytokine secretion profiles in THP-1 cells stimulated with pooled clinical samples and purified LPS controls, with and without modulation by LL-37 and polymyxin B. Data are presented as mean ± SD. Statistical significance relative to the corresponding untreated condition was determined using a paired t -test adjusted for multiple comparisons via the Benjamini-Hochberg method (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
    Figure Legend Snippet: Cytokine secretion profiles in THP-1 cells stimulated with pooled clinical samples and purified LPS controls, with and without modulation by LL-37 and polymyxin B. Data are presented as mean ± SD. Statistical significance relative to the corresponding untreated condition was determined using a paired t -test adjusted for multiple comparisons via the Benjamini-Hochberg method (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Techniques Used: Purification



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    Image Search Results


    Modulation of NF-κB and IRF signaling pathways in THP-1 Dual cells by LL-37 and Polymyxin B. (A) NF-κB activity quantified using the Quanti-Blue assay. (B) IRF activity measured using the Quanti-Luc assay. Data represent mean ± SD. Statistical significance relative to the untreated condition was determined using a paired t -test with Benjamini-Hochberg correction for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Journal: Frontiers in Microbiology

    Article Title: Modulation of LPS-associated virulence activity for reduction of periodontal inflammatory burden

    doi: 10.3389/fmicb.2026.1728315

    Figure Lengend Snippet: Modulation of NF-κB and IRF signaling pathways in THP-1 Dual cells by LL-37 and Polymyxin B. (A) NF-κB activity quantified using the Quanti-Blue assay. (B) IRF activity measured using the Quanti-Luc assay. Data represent mean ± SD. Statistical significance relative to the untreated condition was determined using a paired t -test with Benjamini-Hochberg correction for multiple comparisons (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Article Snippet: THP-1 monocytes and THP-1 DualTM reporter cells (InvivoGen, US) were cultured in RPMI-1640 medium supplemented with 10% heat-inactivated fetal bovine serum and 1% penicillin–streptomycin and then equilibrated in antibiotic-free medium before stimulation.

    Techniques: Protein-Protein interactions, Activity Assay

    Cytokine secretion profiles in THP-1 cells stimulated with pooled clinical samples and purified LPS controls, with and without modulation by LL-37 and polymyxin B. Data are presented as mean ± SD. Statistical significance relative to the corresponding untreated condition was determined using a paired t -test adjusted for multiple comparisons via the Benjamini-Hochberg method (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Journal: Frontiers in Microbiology

    Article Title: Modulation of LPS-associated virulence activity for reduction of periodontal inflammatory burden

    doi: 10.3389/fmicb.2026.1728315

    Figure Lengend Snippet: Cytokine secretion profiles in THP-1 cells stimulated with pooled clinical samples and purified LPS controls, with and without modulation by LL-37 and polymyxin B. Data are presented as mean ± SD. Statistical significance relative to the corresponding untreated condition was determined using a paired t -test adjusted for multiple comparisons via the Benjamini-Hochberg method (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Article Snippet: THP-1 monocytes and THP-1 DualTM reporter cells (InvivoGen, US) were cultured in RPMI-1640 medium supplemented with 10% heat-inactivated fetal bovine serum and 1% penicillin–streptomycin and then equilibrated in antibiotic-free medium before stimulation.

    Techniques: Purification