Review



primary antibodies for ddr2  (Santa Cruz Biotechnology)


Bioz Verified Symbol Santa Cruz Biotechnology is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Santa Cruz Biotechnology primary antibodies for ddr2
    Primary Antibodies For Ddr2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+antibodies+for+ddr2/anti+ddr2/pm36243159-79-8-25
    Average 90 stars, based on 1 article reviews
    primary antibodies for ddr2 - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: Fabrication, characterization and in vivo assessment of cardiogel loaded chitosan patch for myocardial regeneration.
    Article Snippet: Cell therapy is one of the promising approaches for cardiac repair, subsequently after infarction or injury.. However, contemporary mesenchymal stromal/stem cell (MSCs) delivery strategies result in low retention and poor engraftment of donor cells, thus limiting the therapeutic efficacy.. Here, we developed an engineered biomimetic cardiogel patch (EBCP) comprising of the native decellularized cardiac extracellular matrix (ECM) “cardiogel” and chitosan, leading to the efficient regeneration of injured myocardium.



    Similar Products

    primary anti ddr2  (Cell Signaling Technology Inc)
    94
    Cell Signaling Technology Inc primary anti ddr2
    Primary Anti Ddr2, supplied by Cell Signaling Technology Inc, 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/primary+antibodies+for+ddr2/DDR2+Antibody/pmc11816174-55-0-32
    Average 94 stars, based on 1 article reviews
    primary anti ddr2 - by Bioz Stars, 2026-11
    94/100 stars
    		  Buy from Supplier
    primary antibodies against ddr2  (Cell Signaling Technology Inc)
    94
    Cell Signaling Technology Inc primary antibodies against ddr2
    Primary Antibodies Against Ddr2, supplied by Cell Signaling Technology Inc, 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/primary+antibodies+for+ddr2/DDR2+Antibody/pm36614028-241-0-15
    Average 94 stars, based on 1 article reviews
    primary antibodies against ddr2 - by Bioz Stars, 2026-11
    94/100 stars
    		  Buy from Supplier
    primary antibodies for ddr2  (Santa Cruz Biotechnology)
    90
    Santa Cruz Biotechnology primary antibodies for ddr2
    Primary Antibodies For Ddr2, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+antibodies+for+ddr2/anti+ddr2/pm36243159-79-8-25
    Average 90 stars, based on 1 article reviews
    primary antibodies for ddr2 - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier
    primary antibody against ddr2  (Cell Signaling Technology Inc)
    94
    Cell Signaling Technology Inc primary antibody against ddr2
    Cells were pre-treated with metformin hydrochloride (10 μM), 45 mins prior to HG supplementation. (A) <t>DDR2</t> mRNA levels were determined by Taqman real-time PCR at 6 h post-HG treatment, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG (One-way ANOVA p< 0.05). (B) Protein was isolated after 12h of HG treatment and subjected to western blot analysis for detection of DDR2, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).
    Primary Antibody Against Ddr2, supplied by Cell Signaling Technology Inc, 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/primary+antibodies+for+ddr2/DDR2+Antibody/bio_rxiv__2022__10__24__513528-77-0-15
    Average 94 stars, based on 1 article reviews
    primary antibody against ddr2 - by Bioz Stars, 2026-11
    94/100 stars
    		  Buy from Supplier

    Image Search Results


    Cells were pre-treated with metformin hydrochloride (10 μM), 45 mins prior to HG supplementation. (A) DDR2 mRNA levels were determined by Taqman real-time PCR at 6 h post-HG treatment, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG (One-way ANOVA p< 0.05). (B) Protein was isolated after 12h of HG treatment and subjected to western blot analysis for detection of DDR2, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Journal: bioRxiv

    Article Title: Metformin attenuates hyperglycaemia-stimulated pro-fibrotic gene expression in vascular adventitial fibroblasts via inhibition of Discoidin Domain Receptor 2

    doi: 10.1101/2022.10.24.513528

    Figure Lengend Snippet: Cells were pre-treated with metformin hydrochloride (10 μM), 45 mins prior to HG supplementation. (A) DDR2 mRNA levels were determined by Taqman real-time PCR at 6 h post-HG treatment, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG (One-way ANOVA p< 0.05). (B) Protein was isolated after 12h of HG treatment and subjected to western blot analysis for detection of DDR2, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Article Snippet: Primary antibody against DDR2 (Cat No. 12133S) and TGF-β1 (Cat No. 3711) were obtained from Cell Signalling Technology (Danvers, MA, USA).

    Techniques: Real-time Polymerase Chain Reaction, Control, Isolation, Western Blot

    Vascular adventitial fibroblasts were transiently transfected with DDR2 siRNA or scrambled siRNA. Following exposure of the transfected cells to HG for 12 h, fibronectin protein expression was examined by western blot analysis and normalized to β-actin. **p< 0.005 vs. control, #p< 0.05 vs. HG. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Journal: bioRxiv

    Article Title: Metformin attenuates hyperglycaemia-stimulated pro-fibrotic gene expression in vascular adventitial fibroblasts via inhibition of Discoidin Domain Receptor 2

    doi: 10.1101/2022.10.24.513528

    Figure Lengend Snippet: Vascular adventitial fibroblasts were transiently transfected with DDR2 siRNA or scrambled siRNA. Following exposure of the transfected cells to HG for 12 h, fibronectin protein expression was examined by western blot analysis and normalized to β-actin. **p< 0.005 vs. control, #p< 0.05 vs. HG. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Article Snippet: Primary antibody against DDR2 (Cat No. 12133S) and TGF-β1 (Cat No. 3711) were obtained from Cell Signalling Technology (Danvers, MA, USA).

    Techniques: Transfection, Expressing, Western Blot, Control

    (A) Vascular adventitial fibroblasts were transiently transfected with TGF-β1 siRNA 1 and 2 (5 pmol each) or scrambled siRNA prior to treatment with HG for 12 h. Protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. Validation of TGF-β1 knockdown is also shown. **p< 0.005 vs. control, ##p< 0.005 vs. HG and ns -not significant vs. control. (B) Sub-confluent, quiescent cultures of vascular adventitial fibroblasts in M199 were pre-treated with SMAD2 inhibitor, PD169316, or SMAD3 inhibitor, SIS3, for 1 h and subsequently with HG for 12 h. Following treatment with HG, protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG and ns - not significant vs. control. (C) Vascular adventitial fibroblasts were co-transfected with DDR2 plasmid (1μg) and TGF-β1 siRNA 1 and 2 (5 pmol each) (lipofectamine 2000-complexed) for 8 h in OptiMEM. After a recovery period of 12 h, the cells were subjected to HG for 12 h. Following treatment with HG, protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. Validation of DDR2 OE and TGF-β1 knockdown is also shown. **p<0.005 vs. Control, ##p<0.005 vs. HG, !!p<0.005 vs. HG + TGF-β siRNA. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Journal: bioRxiv

    Article Title: Metformin attenuates hyperglycaemia-stimulated pro-fibrotic gene expression in vascular adventitial fibroblasts via inhibition of Discoidin Domain Receptor 2

    doi: 10.1101/2022.10.24.513528

    Figure Lengend Snippet: (A) Vascular adventitial fibroblasts were transiently transfected with TGF-β1 siRNA 1 and 2 (5 pmol each) or scrambled siRNA prior to treatment with HG for 12 h. Protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. Validation of TGF-β1 knockdown is also shown. **p< 0.005 vs. control, ##p< 0.005 vs. HG and ns -not significant vs. control. (B) Sub-confluent, quiescent cultures of vascular adventitial fibroblasts in M199 were pre-treated with SMAD2 inhibitor, PD169316, or SMAD3 inhibitor, SIS3, for 1 h and subsequently with HG for 12 h. Following treatment with HG, protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. **p< 0.005 vs. control, ##p< 0.005 vs. HG and ns - not significant vs. control. (C) Vascular adventitial fibroblasts were co-transfected with DDR2 plasmid (1μg) and TGF-β1 siRNA 1 and 2 (5 pmol each) (lipofectamine 2000-complexed) for 8 h in OptiMEM. After a recovery period of 12 h, the cells were subjected to HG for 12 h. Following treatment with HG, protein was isolated and subjected to western blot analysis for detection of fibronectin, with β-actin as loading control. Validation of DDR2 OE and TGF-β1 knockdown is also shown. **p<0.005 vs. Control, ##p<0.005 vs. HG, !!p<0.005 vs. HG + TGF-β siRNA. Data are representative of 3 independent experiments, n=3. Error bars represent Standard Error (SE).

    Article Snippet: Primary antibody against DDR2 (Cat No. 12133S) and TGF-β1 (Cat No. 3711) were obtained from Cell Signalling Technology (Danvers, MA, USA).

    Techniques: Transfection, Isolation, Western Blot, Control, Biomarker Discovery, Knockdown, Plasmid Preparation