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tlr4 specific inhibitor tak242  (TargetMol)


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    Structured Review

    TargetMol tlr4 specific inhibitor tak242
    Tlr4 Specific Inhibitor Tak242, supplied by TargetMol, used in various techniques. Bioz Stars score: 94/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tlr4+specific+inhibitor+tak242/Resatorvid/pm39550424-180-39-43
    Average 94 stars, based on 11 article reviews
    tlr4 specific inhibitor tak242 - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Saline:

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Negative Control:

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Recombinant:

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Western Blot:

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Expressing:

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages.
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..

    Article Title: A novel role of peroxiredoxin 2 in diabetic kidney disease progression by activating the classically activated macrophages
    Article Snippet: .. After full adherence and stretch, cells were treated with phosphate buffered saline (PBS) in the negative control group (NC group), with 5 μg/mL recombinant PRDX2 (HZbscience, HZF757Mu01) in the PRDX2 group and pre-treatment with or without 1 μM of TLR4 specific inhibitor TAK242 (Targetmol, TQ0181) for 1 h. After 12 or 24 h, cells were collected for WB analysis to detect the protein expression level of M1 and M2 polarization related protein. ..



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    Millipore tlr4-specific inhibitor tak242
    APM inhibits LPS-induced CD11b and TNFα expression by inhibiting TLR4 in BV and rat primary microglial cells. Cells were treated with APM for 1 h followed by LPS for 12 h. CD11b and TNFα expression were significantly inhibited in LPS-stimulated BV2 ( A ) and rat primary microglial cells ( B ) by TLR4 inhibitor, <t>TAK242.</t> Cells were treated with APM for 1 h followed by LPS for 6 h. APM significantly reduced LPS-induced TLR4 expression in BV2 ( C ) and rat primary microglial cells ( D ). Immunofluorescence double staining for TLR4 (green) and TNFα (red) localization ( E ) in BV2 microglial cells. Cell were counterstained with DAPI (blue). Magnification 400×. Enlarge figure of scale bars: 5 μm. βActin was used to confirm equal sample loading. CD11b, TNFα and TLR4 followed by densitometric analysis. The data are representative of three independent experiments and quantified as mean values ± SEM. Tukey’s multiple comparison test, * p < 0.05, ** p < 0.01, *** p < 0.001 compared to normal control.
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    Image Search Results


    APM inhibits LPS-induced CD11b and TNFα expression by inhibiting TLR4 in BV and rat primary microglial cells. Cells were treated with APM for 1 h followed by LPS for 12 h. CD11b and TNFα expression were significantly inhibited in LPS-stimulated BV2 ( A ) and rat primary microglial cells ( B ) by TLR4 inhibitor, TAK242. Cells were treated with APM for 1 h followed by LPS for 6 h. APM significantly reduced LPS-induced TLR4 expression in BV2 ( C ) and rat primary microglial cells ( D ). Immunofluorescence double staining for TLR4 (green) and TNFα (red) localization ( E ) in BV2 microglial cells. Cell were counterstained with DAPI (blue). Magnification 400×. Enlarge figure of scale bars: 5 μm. βActin was used to confirm equal sample loading. CD11b, TNFα and TLR4 followed by densitometric analysis. The data are representative of three independent experiments and quantified as mean values ± SEM. Tukey’s multiple comparison test, * p < 0.05, ** p < 0.01, *** p < 0.001 compared to normal control.

    Journal: International Journal of Molecular Sciences

    Article Title: Apamin Suppresses LPS-Induced Neuroinflammatory Responses by Regulating SK Channels and TLR4-Mediated Signaling Pathways

    doi: 10.3390/ijms21124319

    Figure Lengend Snippet: APM inhibits LPS-induced CD11b and TNFα expression by inhibiting TLR4 in BV and rat primary microglial cells. Cells were treated with APM for 1 h followed by LPS for 12 h. CD11b and TNFα expression were significantly inhibited in LPS-stimulated BV2 ( A ) and rat primary microglial cells ( B ) by TLR4 inhibitor, TAK242. Cells were treated with APM for 1 h followed by LPS for 6 h. APM significantly reduced LPS-induced TLR4 expression in BV2 ( C ) and rat primary microglial cells ( D ). Immunofluorescence double staining for TLR4 (green) and TNFα (red) localization ( E ) in BV2 microglial cells. Cell were counterstained with DAPI (blue). Magnification 400×. Enlarge figure of scale bars: 5 μm. βActin was used to confirm equal sample loading. CD11b, TNFα and TLR4 followed by densitometric analysis. The data are representative of three independent experiments and quantified as mean values ± SEM. Tukey’s multiple comparison test, * p < 0.05, ** p < 0.01, *** p < 0.001 compared to normal control.

    Article Snippet: Cells were pretreated with various inhibitors such as TLR4-specific inhibitor (Millipore, Bedford, MA, USA): TAK242 (500 nM), NF-κB-specific inhibitor (Sigma-Aldrich): Bay11-7085 (10 μM), STAT3-specific inhibitor (Sigma-Aldrich): S3I-201 (10 μM) and ERK1/2-specific inhibitor (Cell signaling, Danvers, MA, USA): PD98059 (10 μM).

    Techniques: Expressing, Immunofluorescence, Double Staining, Comparison, Control