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mmp14  (Proteintech)


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    Structured Review

    Proteintech mmp14
    Mmp14, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 55 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mmp14/MT1-MMP+Antibody/pm41673566-117-296-302
    Average 93 stars, based on 55 article reviews
    mmp14 - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Incubation:

    Article Title: Network pharmacology and in vitro experiments reveal the potential therapeutic effects of Scrophularia ningpoensis Hemsl in the treatment of ameloblastoma.
    Article Snippet: Purpose: This study aimed to explore active ingredients in Scrophularia ningpoensis Hemsl (SNH) with potential effects on ameloblastoma (AM) using network pharmacological approach, bioinformatic gene analysis and in vitro cell experiments.. Methods: The active ingredients and their corresponding targets of SNH were identified from the Traditional Chinese Medicine Systems Pharmacology (TCMSP), as well as SwissTargetPrediction.. Disease targets of AM were selected from GeneCards and DisGeNET databases.

    Article Title: Matrix metalloproteinases are hallmark early biomarkers and therapeutic targets in FSHD
    Article Snippet: .. For immunofluorescence, tissue sections or sorted FAPs were fixed in 4% PFA for 10 minutes, permeabilized with 0.3% Triton X-100 for 30 minutes, and incubated overnight at 4°C with primary antibody against collagen VI (1:200, Proteintech), MMP2 (1:500, Proteintech), MMP14 (1:500, Proteintech), PDGFRα (1:200, BioLegend), F4/80 (1:200, BioLegend), and Ki-67 (1:400, BioLegend), followed by secondary antibody conjugate to Alexa Fluor 488, 555, or 647 (1:500, Thermo Fisher Scientific) for 2 hours at room temperature. .. Nuclei were visualized with DAPI (1:5,000, Sigma).

    Ubiquitin Proteomics:

    Article Title: Neoadjuvant Chemotherapy With Cisplatin Up‐Regulates GSDMD to Enhance Oral Squamous Cell Carcinoma Metastasis Through MMP14‐Mediated EMT Activation
    Article Snippet: Antibodies specific for DYKDDDDK (FLAG tag, #14 793) and GAPDH (#5174), anti‐rabbit IgG (#7074), and anti‐mouse IgG (#7076) were purchased from Cell Signaling Technology. .. Antibodies specific for GSDMD (20770‐1‐AP), MMP14 (14552‐1‐AP), vimentin (60330‐1‐Ig), E‐cadherin (20874‐1‐AP), N‐cadherin (22018‐1‐AP), MMP2 (10373‐1‐AP), MMP‐9 (10375‐2‐AP), SNAIL2 (13099‐1‐AP), ubiquitin (10201‐2‐AP), Ki67 (27309‐1‐AP), and mCherry (26765‐1‐AP) were purchased from Proteintech. ..

    Article Title: Neoadjuvant Chemotherapy With Cisplatin Up-Regulates GSDMD to Enhance Oral Squamous Cell Carcinoma Metastasis Through MMP14-Mediated EMT Activation.
    Article Snippet: Antibodies and Reagents: Antibodies specific for DYKDDDDK (FLAG tag, #14 793) and GAPDH (#5174), anti-rabbit IgG (#7074), and antimouse IgG (#7076) were purchased from Cell Signaling Technology. .. Antibodies specific for GSDMD (20770-1-AP), MMP14 (14552-1-AP), vimentin (60330-1-Ig), E-cadherin (20874-1-AP), N-cadherin (22018-1-AP), MMP2 (10373-1-AP), MMP-9 (10375-2-AP), SNAIL2 (13099-1-AP), ubiquitin (10201-2-AP), Ki67 (27309-1-AP), and mCherry (26765-1-AP) were purchased from Proteintech. ..

    Concentration Assay:

    Article Title: The promoting roles of GLP1R and GIPR in stemness maintenance and multiple lineage-specific differentiation of PDLSCs
    Article Snippet: .. The information and the concentration of antibodies used in this study were listed as follows: Phospho-(Ser/Thr) PKA substrate antibody (1: 500, cat. no. 9621, CST, USA), GLP1R (1: 2,000, cat. no. 26196-1-AP, Proteintech, China), GIPR (1: 2,000, cat. no. 28322-1-AP, Proteintech), STRO-1 (1: 250, cat. no. 39-8401, Thermo Fisher Scientific), CD146 (1: 2,000, cat. no. 65181-1-Ig, Proteintech), Vimentin (1: 2,000, cat. no. 10366-1-AP, Proteintech), CREB1 (1: 2,000, cat. no. 67927-1-Ig, Proteintech), p-CREB1 (Ser133) (1: 2,000, cat. no. 28792-1-AP, Proteintech), ERK1/2 (1: 2,000, cat. no. 66192-1-Ig, Proteintech), p-ERK1/2 (Thr202/Tyr204) (1: 2,000, cat. no. 28733-1-AP, Proteintech), β-catenin (1: 2,000, cat. no. 51067-2-AP, Proteintech), p-β-catenin (Ser33) (1: 2,000, cat. no. 80067-1-RR, Proteintech), STAT3 (1: 2,000, cat. no. 10253-2-AP, Proteintech), p-STAT3 (Ser727) (1: 2,000, cat. no. 80199-2-RR, Proteintech), Ki-67 (1: 2,000, cat. no. 84192-4-RR, Proteintech), PCNA (1: 2,000, cat. no. 10205-2-AP, Proteintech), CCND3 (1: 2,000, cat. no. 26755-1-AP, Proteintech), β-actin (1: 2,000, cat. no. 66009-1- Ig, Proteintech), COL1A1 (1: 2,000, cat. no. 67288-1-Ig, Proteintech), OCN (1: 2,000, cat. no. 20277-1-AP, Proteintech), RUNX2 (1: 2,000, cat. no. 20700-1-AP, Proteintech), C/EBPα (1: 2,000, cat. no. 29388-1-AP, Proteintech), FABP4 (1: 2,000, cat. no. 12802-1-AP, Proteintech), PPARγ (1: 2,000, cat. no. 16643-1-AP, Proteintech), ACAN (1: 2,000, cat. no. 68350-1-Ig, Proteintech), COL2A1 (1: 2,000, cat. no. 28459-1-AP, Proteintech), SOX9 (1: 2,000, cat. no. 67439-1-Ig, Proteintech), MAP2 (1: 2,000, cat. no. 17490-1-AP, Proteintech), Nestin (1: 2,000, cat. no. 19483-1-AP, Proteintech), TUBB3 (1: 2,000, cat. no. 66375-1-Ig, Proteintech), IFIT1 (1: 2,000, cat. no. ab305301, Abcam), IFIT2 (1: 2,000, cat. no. 12604-1-AP, Proteintech), IFIT3 (1: 2,000, cat. no. 15201-1-AP, Proteintech), eIF3C (1: 2,000, cat. no. 12733-1-AP, Proteintech), eIF3E (1: 2,000, cat. no. 10899-1-AP, Proteintech), RPS3 (1: 2,000, cat. no. 66046-1-Ig, Proteintech), SPP1 (1: 2,000, cat. no. 22952-1-AP, Proteintech), FGF18 (1: 2,000, cat. no. 11495-1-AP, Proteintech), MMP14 (1: 2,000, cat. no. 14552-1-AP, Proteintech), BMP2 (1: 2,000, cat. no. 66383-1-Ig, Proteintech), horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG (1: 5,000, cat. no. SA00001-2, Proteintech), and HRP-conjugated goat anti-mouse IgG (1: 5,000, cat. no. SA00001-1, Proteintech). ..

    Article Title: The promoting roles of GLP1R and GIPR in stemness maintenance and multiple lineage-specific differentiation of PDLSCs.
    Article Snippet: .. The information and the concentration of antibodies used in this study were listed as follows: Phospho-(Ser/Thr) PKA substrate antibody (1: 500, cat. no. 9621, CST, USA), GLP1R (1: 2,000, cat. no. 26196-1-AP, Proteintech, China), GIPR (1: 2,000, cat. no. 28322-1-AP, Proteintech), STRO-1 (1: 250, cat. no. 39-8401, Thermo Fisher Scientific), CD146 (1: 2,000, cat. no. 65181-1-Ig, Proteintech), Vimentin (1: 2,000, cat. no. 10366-1-AP, Proteintech), CREB1 (1: 2,000, cat. no. 67927-1-Ig, Proteintech), p-CREB1 (Ser133) (1: 2,000, cat. no. 28792-1-AP, Proteintech), ERK1/2 (1: 2,000, cat. no. 66192-1-Ig, Proteintech), p-ERK1/2 (Thr202/Tyr204) (1: 2,000, cat. no. 28733-1-AP, Proteintech), β-catenin (1: 2,000, cat. no. 51067-2-AP, Proteintech), p-β-catenin (Ser33) (1: 2,000, cat. no. 80067-1-RR, Proteintech), STAT3 (1: 2,000, cat. no. 10253-2-AP, Proteintech), p-STAT3 (Ser727) (1: 2,000, cat. no. 80199-2-RR, Proteintech), Ki-67 (1: 2,000, cat. no. 84192-4-RR, Proteintech), PCNA (1: 2,000, cat. no. 10205-2-AP, Proteintech), CCND3 (1: 2,000, cat. no. 26755-1- AP, Proteintech), β-actin (1: 2,000, cat. no. 66009-1- Ig, Proteintech), COL1A1 (1: 2,000, cat. no. 67288-1-Ig, Proteintech), OCN (1: 2,000, cat. no. 20277-1-AP, Proteintech), RUNX2 (1: 2,000, cat. no. 20700-1-AP, Proteintech), C/EBPα (1: 2,000, cat. no. 29388- 1-AP, Proteintech), FABP4 (1: 2,000, cat. no. 12802-1-AP, Proteintech), PPARγ (1: 2,000, cat. no. 16643-1-AP, Proteintech), ACAN (1: 2,000, cat. no. 68350-1-Ig, Proteintech), COL2A1 (1: 2,000, cat. no. 28459-1-AP, Proteintech), SOX9 (1: 2,000, cat. no. 67439-1- Ig, Proteintech), MAP2 (1: 2,000, cat. no. 17490-1-AP, Proteintech), Nestin (1: 2,000, cat. no. 19483-1-AP, Proteintech), TUBB3 (1: 2,000, cat. no. 66375-1-Ig, Proteintech), IFIT1 (1: 2,000, cat. no. ab305301, Abcam), IFIT2 (1: 2,000, cat. no. 12604-1-AP, Proteintech), IFIT3 (1: 2,000, cat. no. 15201-1-AP, Proteintech), eIF3C (1: 2,000, cat. no. 12733-1-AP, Proteintech), eIF3E (1: 2,000, cat. no. 10899-1-AP, Proteintech), RPS3 (1: 2,000, cat. no. 66046-1-Ig, Proteintech), SPP1 (1: 2,000, cat. no. 22952-1-AP, Proteintech), FGF18 (1: 2,000, cat. no. 11495-1-AP, Proteintech), MMP14 (1: 2,000, cat. no. 14552-1-AP, Proteintech), BMP2 (1: 2,000, cat. no. 66383-1-Ig, Proteintech), horseradish peroxidase (HRP)-conjugated goat anti-rabbit IgG (1: 5,000, cat. no. SA00001-2, Proteintech), and HRP-conjugated goat anti-mouse IgG (1: 5,000, cat. no. SA00001-1, Proteintech). ..

    Western Blot:

    Article Title: TMED9: a potential therapeutic target and prognostic marker in glioma and its implications across pan-cancer contexts
    Article Snippet: Protease inhibitors (Solarbio, China) were added to RIPA buffer to prepare total protein extracts. .. Antibodies for TMED9, GAPDH, MMP14, Vimentin, and MMP2 were obtained from Proteintech (China) and employed according to the manufacturer’s instructions for Western blot analysis. .. Goat Anti-Rabbit IgG-HRP (Proteintech, China) served as the secondary antibody.

    Immunofluorescence:

    Article Title: Matrix metalloproteinases are hallmark early biomarkers and therapeutic targets in FSHD
    Article Snippet: .. For immunofluorescence, tissue sections or sorted FAPs were fixed in 4% PFA for 10 minutes, permeabilized with 0.3% Triton X-100 for 30 minutes, and incubated overnight at 4°C with primary antibody against collagen VI (1:200, Proteintech), MMP2 (1:500, Proteintech), MMP14 (1:500, Proteintech), PDGFRα (1:200, BioLegend), F4/80 (1:200, BioLegend), and Ki-67 (1:400, BioLegend), followed by secondary antibody conjugate to Alexa Fluor 488, 555, or 647 (1:500, Thermo Fisher Scientific) for 2 hours at room temperature. .. Nuclei were visualized with DAPI (1:5,000, Sigma).



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    ( A ) UMAP plot showing annotated cell clusters. Major cell types are labeled and color-coded, including epithelial, immune, endothelial, and stromal populations. MMP expression was determined in 32 different cell types. ( B ) UMAP plots showing the expression of selected MMP genes (MMP10, 11, 15, 16, 17, 20, 21, 23, 24, 25, 27, 28) in single cells from mouse lung tissue (filtered air group, n = 9). Expression is color-coded by log-normalized expression levels, with darker shades indicating higher expression. ( C – E ) qRT-PCR data showing mRNA expression levels of Mmp1a, Mmp1b, Mmp2, Mmp3, Mmp9, Mmp12, Mmp13, <t>Mmp14,</t> and Mmp19 in pmLF, IMΦ or AMΦ (WT and Trpml1 −/− ). ( F ) qRT-PCR data showing mRNA expression levels of Timp1, Timp2, Timp3, Timp4 in pmLF and IMΦ (WT and Trpml1 −/− ). In all figures, each single dot corresponds to one biologically independent sample. Data were mean ± SEM. Statistical analysis for qRT-PCR data were performed with multiple t -test, corrected for multiple comparisons using the Holm–Šídák method. ( G – J ) Western Blot analysis of different MMPs in pmLF isolated from WT and Trpml1 −/− mice. Graphs show quantification of each MMP band normalized to ß-actin. Each single dot corresponds to cells isolated from one mouse. Data were mean ± SEM. Student’s t -test, unpaired, two-tailed. .
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    Image Search Results


    ( A ) UMAP plot showing annotated cell clusters. Major cell types are labeled and color-coded, including epithelial, immune, endothelial, and stromal populations. MMP expression was determined in 32 different cell types. ( B ) UMAP plots showing the expression of selected MMP genes (MMP10, 11, 15, 16, 17, 20, 21, 23, 24, 25, 27, 28) in single cells from mouse lung tissue (filtered air group, n = 9). Expression is color-coded by log-normalized expression levels, with darker shades indicating higher expression. ( C – E ) qRT-PCR data showing mRNA expression levels of Mmp1a, Mmp1b, Mmp2, Mmp3, Mmp9, Mmp12, Mmp13, Mmp14, and Mmp19 in pmLF, IMΦ or AMΦ (WT and Trpml1 −/− ). ( F ) qRT-PCR data showing mRNA expression levels of Timp1, Timp2, Timp3, Timp4 in pmLF and IMΦ (WT and Trpml1 −/− ). In all figures, each single dot corresponds to one biologically independent sample. Data were mean ± SEM. Statistical analysis for qRT-PCR data were performed with multiple t -test, corrected for multiple comparisons using the Holm–Šídák method. ( G – J ) Western Blot analysis of different MMPs in pmLF isolated from WT and Trpml1 −/− mice. Graphs show quantification of each MMP band normalized to ß-actin. Each single dot corresponds to cells isolated from one mouse. Data were mean ± SEM. Student’s t -test, unpaired, two-tailed. .

    Journal: The EMBO Journal

    Article Title: TRPML1 suppresses pulmonary fibrosis by limiting collagen and elastin deposition

    doi: 10.1038/s44318-026-00712-4

    Figure Lengend Snippet: ( A ) UMAP plot showing annotated cell clusters. Major cell types are labeled and color-coded, including epithelial, immune, endothelial, and stromal populations. MMP expression was determined in 32 different cell types. ( B ) UMAP plots showing the expression of selected MMP genes (MMP10, 11, 15, 16, 17, 20, 21, 23, 24, 25, 27, 28) in single cells from mouse lung tissue (filtered air group, n = 9). Expression is color-coded by log-normalized expression levels, with darker shades indicating higher expression. ( C – E ) qRT-PCR data showing mRNA expression levels of Mmp1a, Mmp1b, Mmp2, Mmp3, Mmp9, Mmp12, Mmp13, Mmp14, and Mmp19 in pmLF, IMΦ or AMΦ (WT and Trpml1 −/− ). ( F ) qRT-PCR data showing mRNA expression levels of Timp1, Timp2, Timp3, Timp4 in pmLF and IMΦ (WT and Trpml1 −/− ). In all figures, each single dot corresponds to one biologically independent sample. Data were mean ± SEM. Statistical analysis for qRT-PCR data were performed with multiple t -test, corrected for multiple comparisons using the Holm–Šídák method. ( G – J ) Western Blot analysis of different MMPs in pmLF isolated from WT and Trpml1 −/− mice. Graphs show quantification of each MMP band normalized to ß-actin. Each single dot corresponds to cells isolated from one mouse. Data were mean ± SEM. Student’s t -test, unpaired, two-tailed. .

    Article Snippet: MMP14 ELISA kit , Novus biologicals , NBP3-06941.

    Techniques: Labeling, Expressing, Quantitative RT-PCR, Western Blot, Isolation, Two Tailed Test

    ( A ) UMAP plot showing annotated cell clusters. Major cell types are labeled and color-coded, including epithelial, immune, endothelial, and stromal populations. MMP expression was determined in 32 different cell types. ( B ) UMAP plots showing the expression of selected MMP genes (MMP10, 11, 15, 16, 17, 20, 21, 23, 24, 25, 27, 28) in single cells from mouse lung tissue (filtered air group, n = 9). Expression is color-coded by log-normalized expression levels, with darker shades indicating higher expression. ( C – E ) qRT-PCR data showing mRNA expression levels of Mmp1a, Mmp1b, Mmp2, Mmp3, Mmp9, Mmp12, Mmp13, Mmp14, and Mmp19 in pmLF, IMΦ or AMΦ (WT and Trpml1 −/− ). ( F ) qRT-PCR data showing mRNA expression levels of Timp1, Timp2, Timp3, Timp4 in pmLF and IMΦ (WT and Trpml1 −/− ). In all figures, each single dot corresponds to one biologically independent sample. Data were mean ± SEM. Statistical analysis for qRT-PCR data were performed with multiple t -test, corrected for multiple comparisons using the Holm–Šídák method. ( G – J ) Western Blot analysis of different MMPs in pmLF isolated from WT and Trpml1 −/− mice. Graphs show quantification of each MMP band normalized to ß-actin. Each single dot corresponds to cells isolated from one mouse. Data were mean ± SEM. Student’s t -test, unpaired, two-tailed. .

    Journal: The EMBO Journal

    Article Title: TRPML1 suppresses pulmonary fibrosis by limiting collagen and elastin deposition

    doi: 10.1038/s44318-026-00712-4

    Figure Lengend Snippet: ( A ) UMAP plot showing annotated cell clusters. Major cell types are labeled and color-coded, including epithelial, immune, endothelial, and stromal populations. MMP expression was determined in 32 different cell types. ( B ) UMAP plots showing the expression of selected MMP genes (MMP10, 11, 15, 16, 17, 20, 21, 23, 24, 25, 27, 28) in single cells from mouse lung tissue (filtered air group, n = 9). Expression is color-coded by log-normalized expression levels, with darker shades indicating higher expression. ( C – E ) qRT-PCR data showing mRNA expression levels of Mmp1a, Mmp1b, Mmp2, Mmp3, Mmp9, Mmp12, Mmp13, Mmp14, and Mmp19 in pmLF, IMΦ or AMΦ (WT and Trpml1 −/− ). ( F ) qRT-PCR data showing mRNA expression levels of Timp1, Timp2, Timp3, Timp4 in pmLF and IMΦ (WT and Trpml1 −/− ). In all figures, each single dot corresponds to one biologically independent sample. Data were mean ± SEM. Statistical analysis for qRT-PCR data were performed with multiple t -test, corrected for multiple comparisons using the Holm–Šídák method. ( G – J ) Western Blot analysis of different MMPs in pmLF isolated from WT and Trpml1 −/− mice. Graphs show quantification of each MMP band normalized to ß-actin. Each single dot corresponds to cells isolated from one mouse. Data were mean ± SEM. Student’s t -test, unpaired, two-tailed. .

    Article Snippet: The following ELISAs were used for the experiments: SP-A ELISA (NBP2-76693, Novus biologicals), Cathepsin K ELISA (NBP3-00426, Novus biologicals), TIMP1 ELISA (ab196265, Abcam), TIMP2 ELISA (ab227893, Abcam), MMP1 ELISA (NBP3-06885, Novus biologicals and ABIN6963621, Antibodies online), MMP2 ELISA (ab254516, Abcam), MMP3 ELISA (ab100731), MMP8 ELISA (ab206982, Abcam), MMP9 ELISA (MMPT90, R&D systems), MMP12 ELISA (ab213878, Abcam), MMP13 ELISA (NBP3-06930, Novus biologicals), MMP14 ELISA (NBP3-06941, Novus biologicals and ABIN6957687, Antibodies online), MMP19 ELISA (NBP3-06941, Novus biologicals), IL-17A ELISA (ab199081, Abcam), DESMOSINE ELISA (CSB-E14196m, Cusabio).

    Techniques: Labeling, Expressing, Quantitative RT-PCR, Western Blot, Isolation, Two Tailed Test

    Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Journal: International Journal of General Medicine

    Article Title: Exploring the Mechanisms of the Traditional Herbal Formula Sanshen Dan Against Myocardial Ischemia-Reperfusion Injury: An Integrated Strategy Combining Serum Pharmacochemistry, Network Pharmacology, and Molecular Docking

    doi: 10.2147/IJGM.S577525

    Figure Lengend Snippet: Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Article Snippet: Figure 6 Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Techniques:

    Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Journal: International Journal of General Medicine

    Article Title: Exploring the Mechanisms of the Traditional Herbal Formula Sanshen Dan Against Myocardial Ischemia-Reperfusion Injury: An Integrated Strategy Combining Serum Pharmacochemistry, Network Pharmacology, and Molecular Docking

    doi: 10.2147/IJGM.S577525

    Figure Lengend Snippet: Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Article Snippet: Figure 6 Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Techniques:

    Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Journal: International Journal of General Medicine

    Article Title: Exploring the Mechanisms of the Traditional Herbal Formula Sanshen Dan Against Myocardial Ischemia-Reperfusion Injury: An Integrated Strategy Combining Serum Pharmacochemistry, Network Pharmacology, and Molecular Docking

    doi: 10.2147/IJGM.S577525

    Figure Lengend Snippet: Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Article Snippet: Figure 6 Gibbs Free Energy Landscapes of Ligand–Receptor Complexes from Molecular Dynamics Simulations ( A ) Gibbs free energy landscape of the SSD28–Mmp14 complex; ( B ) Gibbs free energy landscape of the SSD43–Mmp14 complex; ( C ) Gibbs free energy landscape of the SSD25–Mmp14 complex; ( D ) Gibbs free energy landscape of the SSD28–Ctnnb1 complex; ( E ) Gibbs free energy landscape of the SSD43–Ctnnb1 complex; ( F ) Gibbs free energy landscape of the SSD14–Ctnnb1 complex.

    Techniques: