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nod2 tlr2 agonist  (InvivoGen)


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    InvivoGen nod2 tlr2 agonist
    Nod2 Tlr2 Agonist, supplied by InvivoGen, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nod2+tlr2+agonist/bio_rxiv__64898__2026__04__11__717924-274-24-26?v=InvivoGen
    Average 94 stars, based on 15 article reviews
    nod2 tlr2 agonist - by Bioz Stars, 2026-08
    94/100 stars

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    (A) Intranasal inoculation of wild-type mice with live (black bars) or heat-inactivated (grey-bars) of L. plantarum followed by evaluation of lung tissue at time points as in Fig. 1; no L. plantarum control is shown in blue at t = 0; n = 3 mice per group. SLP assay as described in Methods, interpolated to a standard curve as in Fig. 2 is generated for each experiment. (B) Intranasal inoculation of wild-type (blue bars) or <t>NOD2-TLR2</t> gene-deleted mice <t>(NOD2−/−TLR2−/−;</t> grey bars) with heat-inactivated L. plantarum followed by evaluation of lung tissue at time points indicate; n = 3 mice per group. (C) Inoculation of wild-type mice with soluble bi-functional pattern-recognition receptor agonist CL-429 (20 µg per mouse in 50 µL pbs/bsa) followed by evaluation of mouse lung tissue at time points indicated; n = 3 - 4 mice per group, *p<0.01, **p < 0.001 by ANOVA.
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    (A) Intranasal inoculation of wild-type mice with live (black bars) or heat-inactivated (grey-bars) of L. plantarum followed by evaluation of lung tissue at time points as in Fig. 1; no L. plantarum control is shown in blue at t = 0; n = 3 mice per group. SLP assay as described in Methods, interpolated to a standard curve as in Fig. 2 is generated for each experiment. (B) Intranasal inoculation of wild-type (blue bars) or NOD2-TLR2 gene-deleted mice (NOD2−/−TLR2−/−; grey bars) with heat-inactivated L. plantarum followed by evaluation of lung tissue at time points indicate; n = 3 mice per group. (C) Inoculation of wild-type mice with soluble bi-functional pattern-recognition receptor agonist CL-429 (20 µg per mouse in 50 µL pbs/bsa) followed by evaluation of mouse lung tissue at time points indicated; n = 3 - 4 mice per group, *p<0.01, **p < 0.001 by ANOVA.

    Journal: Journal of microbiological methods

    Article Title: SILKWORM LARVAE PLASMA (SLP) ASSAY FOR DETECTION OF BACTERIA: FALSE POSITIVES SECONDARY TO INFLAMMATION IN VIVO

    doi: 10.1016/j.mimet.2016.11.009

    Figure Lengend Snippet: (A) Intranasal inoculation of wild-type mice with live (black bars) or heat-inactivated (grey-bars) of L. plantarum followed by evaluation of lung tissue at time points as in Fig. 1; no L. plantarum control is shown in blue at t = 0; n = 3 mice per group. SLP assay as described in Methods, interpolated to a standard curve as in Fig. 2 is generated for each experiment. (B) Intranasal inoculation of wild-type (blue bars) or NOD2-TLR2 gene-deleted mice (NOD2−/−TLR2−/−; grey bars) with heat-inactivated L. plantarum followed by evaluation of lung tissue at time points indicate; n = 3 mice per group. (C) Inoculation of wild-type mice with soluble bi-functional pattern-recognition receptor agonist CL-429 (20 µg per mouse in 50 µL pbs/bsa) followed by evaluation of mouse lung tissue at time points indicated; n = 3 - 4 mice per group, *p<0.01, **p < 0.001 by ANOVA.

    Article Snippet: The bifunctional NOD2-TLR2 agonist, CL-429 (Invivogen) was diluted in PBS/BSA and delivered to isoflurane-anaesthetized mice (20 µg/ 50 µL per mouse) in parallel with appropriate diluent controls.

    Techniques: Generated, Functional Assay