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mmp13 protein levels  (Proteintech)


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    Proteintech mmp13 protein levels
    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted <t>MMP13</t> was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
    Mmp13 Protein Levels, supplied by Proteintech, 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/product/mmp13+protein+levels/pm38251858-99-0-15?v=Proteintech
    Average 94 stars, based on 1 article reviews
    mmp13 protein levels - by Bioz Stars, 2026-08
    94/100 stars

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    1) Product Images from "Breast cancer malignancy is governed by regulation of the macroH2A2/TM4SF1 axis, the AKT/NF-κB pathway, and elevated MMP13 expression."

    Article Title: Breast cancer malignancy is governed by regulation of the macroH2A2/TM4SF1 axis, the AKT/NF-κB pathway, and elevated MMP13 expression.

    Journal: Molecular carcinogenesis

    doi: 10.1002/mc.23683

    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted MMP13 was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
    Figure Legend Snippet: FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted MMP13 was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.

    Techniques Used: Phospho-proteomics, Western Blot, Expressing, Concentration Assay, Software, Enzyme-linked Immunosorbent Assay, Activity Assay, Comparison



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    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted <t>MMP13</t> was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
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    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted <t>MMP13</t> was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
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    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted <t>MMP13</t> was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
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    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted <t>MMP13</t> was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.
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    Image Search Results


    FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted MMP13 was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.

    Journal: Molecular carcinogenesis

    Article Title: Breast cancer malignancy is governed by regulation of the macroH2A2/TM4SF1 axis, the AKT/NF-κB pathway, and elevated MMP13 expression.

    doi: 10.1002/mc.23683

    Figure Lengend Snippet: FIGURE 7 mH2A2/TM4SF1 axis regulates breast cancer cell metastatic potential via the AKT/NF‐κB signaling pathway. (A) Phosphorylation of AKT/NF‐κB was evaluated in NS or shM2 T47D cells using western blot analysis. (B) Protein expression concentration was quantified using Vilber Fusion fx software and presented in a graph. (C, D) Rescue effects of TM4SF1 on AKT/NF‐κB phosphorylation were evaluated using western blot analysis. (E) Secreted MMP13 was quantified using an enzyme‐linked immunosorbent (ELISA) assay. (F) Schematic diagram suggesting the novel role of mH2A2/TM4SF1 axis regulating breast cancer metastasis through the AKT/NF‐κB signaling pathway and MM13P activity. siC, scramble siRNA; siT, siRNA against TM4SF1. (B) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the three groups. (B, D, E) p Values were calculated using one‐way ANOVA with Dunnett's multiple test for comparison between the four groups. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.

    Article Snippet: MMP13 protein levels in culture supernatants were detected using a Human MMP13 ELISA kit (KE00078, Proteintech) according to the manufacturer's instructions. https://onlinelibrary.w iley.com /doi/10.1002/m c.23683 by Indian Institute O f T echnology, W iley O nline L ibrary on [24/01/2024].

    Techniques: Phospho-proteomics, Western Blot, Expressing, Concentration Assay, Software, Enzyme-linked Immunosorbent Assay, Activity Assay, Comparison