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mmp13 protein levels  (R&D Systems)


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    Structured Review

    R&D Systems mmp13 protein levels
    Mmp13 Protein Levels, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 42 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mmp13+protein+levels/Recombinant+Human+MMP-13+Protein%2C+CF/pm23007908-78-2-27
    Average 94 stars, based on 42 article reviews
    mmp13 protein levels - by Bioz Stars, 2026-11
    94/100 stars

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    Construct:

    Article Title: Interleukin-1β modulates endochondral ossification by human adult bone marrow stromal cells.
    Article Snippet: For quantification of calcium deposition, cell layers were harvested and analysed using the RANDOX (Crumlin, Co. Antrim, UK) CA 590 according to the manufacturer’s protocol. .. VEGF and MMP13 protein levels were determined according to manufacturer in total protein lysates collected from constructs cultured for 5 weeks (Quantikine, human VEGF and human pro-MMP13, R&D Systems). .. Total RNA was extracted from cells using TRIzol (Invitrogen/Life Technologies), treated with DNAse and retrotranscribed into cDNA, as previously described (Frank et al., 2002).

    Cell Culture:

    Article Title: Interleukin-1β modulates endochondral ossification by human adult bone marrow stromal cells.
    Article Snippet: For quantification of calcium deposition, cell layers were harvested and analysed using the RANDOX (Crumlin, Co. Antrim, UK) CA 590 according to the manufacturer’s protocol. .. VEGF and MMP13 protein levels were determined according to manufacturer in total protein lysates collected from constructs cultured for 5 weeks (Quantikine, human VEGF and human pro-MMP13, R&D Systems). .. Total RNA was extracted from cells using TRIzol (Invitrogen/Life Technologies), treated with DNAse and retrotranscribed into cDNA, as previously described (Frank et al., 2002).



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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 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