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rabbit anti bovine igg horseradish peroxidase hrpo conjugated antibody  (Bethyl)


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    Structured Review

    Bethyl rabbit anti bovine igg horseradish peroxidase hrpo conjugated antibody
    Rabbit Anti Bovine Igg Horseradish Peroxidase Hrpo Conjugated Antibody, supplied by Bethyl, used in various techniques. Bioz Stars score: 92/100, based on 30 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/a10/pm41753660-96-24-31?v=Bethyl
    Average 92 stars, based on 30 article reviews
    rabbit anti bovine igg horseradish peroxidase hrpo conjugated antibody - by Bioz Stars, 2026-08
    92/100 stars

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    Bethyl rabbit anti bovine igg horseradish peroxidase hrpo conjugated antibody
    The HDAC inhibitor YAK577 reduces CM-induced vascular calcification in VSMCs. ( A ) Chemical structure of YAK577. ( B ) Effect of YAK577 on <t>VSMC</t> viability determined by MTT assay ( n = 4, 5, 5, 5, 4). ( C ) Representative images of Alizarin Red S-stained VSMCs observed under a light microscope. Scale bar = 200 μm. Bottom: Macroscopic photograph of Alizarin Red S-stained VSMCs captured using a smartphone camera, showing red coloration corresponding to calcium deposition. ( D ) Quantitative analysis of calcium content in CM-treated VSMCs with or without YAK577 treatment ( n = 3, 3, 3). Data are presented as mean ± SEM. *** p < 0.001; NS, not significant. GM, growth medium; CM, calcification medium. Each dot represents one independent biological experiment (not a technical replicate).
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    Image Search Results


    The HDAC inhibitor YAK577 reduces CM-induced vascular calcification in VSMCs. ( A ) Chemical structure of YAK577. ( B ) Effect of YAK577 on VSMC viability determined by MTT assay ( n = 4, 5, 5, 5, 4). ( C ) Representative images of Alizarin Red S-stained VSMCs observed under a light microscope. Scale bar = 200 μm. Bottom: Macroscopic photograph of Alizarin Red S-stained VSMCs captured using a smartphone camera, showing red coloration corresponding to calcium deposition. ( D ) Quantitative analysis of calcium content in CM-treated VSMCs with or without YAK577 treatment ( n = 3, 3, 3). Data are presented as mean ± SEM. *** p < 0.001; NS, not significant. GM, growth medium; CM, calcification medium. Each dot represents one independent biological experiment (not a technical replicate).

    Journal: Antioxidants

    Article Title: YAK577 Attenuates Vascular Calcification by Targeting an MMP14–NOX2/ROS Axis in VSMCs and a Vitamin D 3 -Induced Mouse Model

    doi: 10.3390/antiox15050605

    Figure Lengend Snippet: The HDAC inhibitor YAK577 reduces CM-induced vascular calcification in VSMCs. ( A ) Chemical structure of YAK577. ( B ) Effect of YAK577 on VSMC viability determined by MTT assay ( n = 4, 5, 5, 5, 4). ( C ) Representative images of Alizarin Red S-stained VSMCs observed under a light microscope. Scale bar = 200 μm. Bottom: Macroscopic photograph of Alizarin Red S-stained VSMCs captured using a smartphone camera, showing red coloration corresponding to calcium deposition. ( D ) Quantitative analysis of calcium content in CM-treated VSMCs with or without YAK577 treatment ( n = 3, 3, 3). Data are presented as mean ± SEM. *** p < 0.001; NS, not significant. GM, growth medium; CM, calcification medium. Each dot represents one independent biological experiment (not a technical replicate).

    Article Snippet: The rat A10 vascular smooth muscle cell line (ATCC CRL-1476) was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: MTT Assay, Staining, Light Microscopy

    MMP14 overexpression promotes NOX2 upregulation and enhances osteogenic marker expression in A10 cells. ( A – D ) qRT-PCR analysis of Mmp14 ( n = 8, 8), Bmp2 ( n = 10, 8), Runx2 ( n = 10, 8), and Msx2 ( n = 12, 12) mRNA levels in A10 cells following MMP14 plasmid transfection. ( E , F ) Representative Western blots and corresponding densitometric quantification showing increased expression of MMP14 ( n = 7, 7), RUNX2 ( n = 9, 9), BMP2 ( n = 8, 8) and NOX2 ( n = 7, 7) proteins after MMP14 overexpression. β-actin was used as a loading control. ( G ) Representative immunofluorescence images of A10 cells transfected with vector or GFP-MMP14. GFP-MMP14 was detected with anti-GFP antibody/Alexa Fluor 488 (green), F-actin with Texas Red-X Phalloidin (red), and nuclei with DAPI (blue). Scale bar = 100 μm. Data are presented as mean ± SEM. *** p < 0.001; ** p < 0.01; NS, not significant. Each dot represents one independent biological experiment (not a technical replicate).

    Journal: Antioxidants

    Article Title: YAK577 Attenuates Vascular Calcification by Targeting an MMP14–NOX2/ROS Axis in VSMCs and a Vitamin D 3 -Induced Mouse Model

    doi: 10.3390/antiox15050605

    Figure Lengend Snippet: MMP14 overexpression promotes NOX2 upregulation and enhances osteogenic marker expression in A10 cells. ( A – D ) qRT-PCR analysis of Mmp14 ( n = 8, 8), Bmp2 ( n = 10, 8), Runx2 ( n = 10, 8), and Msx2 ( n = 12, 12) mRNA levels in A10 cells following MMP14 plasmid transfection. ( E , F ) Representative Western blots and corresponding densitometric quantification showing increased expression of MMP14 ( n = 7, 7), RUNX2 ( n = 9, 9), BMP2 ( n = 8, 8) and NOX2 ( n = 7, 7) proteins after MMP14 overexpression. β-actin was used as a loading control. ( G ) Representative immunofluorescence images of A10 cells transfected with vector or GFP-MMP14. GFP-MMP14 was detected with anti-GFP antibody/Alexa Fluor 488 (green), F-actin with Texas Red-X Phalloidin (red), and nuclei with DAPI (blue). Scale bar = 100 μm. Data are presented as mean ± SEM. *** p < 0.001; ** p < 0.01; NS, not significant. Each dot represents one independent biological experiment (not a technical replicate).

    Article Snippet: The rat A10 vascular smooth muscle cell line (ATCC CRL-1476) was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Over Expression, Marker, Expressing, Quantitative RT-PCR, Plasmid Preparation, Transfection, Western Blot, Control, Immunofluorescence