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integrinβ1  (Proteintech)


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    Proteintech integrinβ1
    Integrinβ1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 225 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+integrin%CE%B21/Integrin+beta-1+Antibody/pm41923217-130-18-19
    Average 96 stars, based on 225 article reviews
    integrinβ1 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Incubation:

    Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro
    Article Snippet: .. Then, the following primary antibodies were added and incubated overnight at 4°C: anti-FGL1 (1:500, 16000-1-AP, Proteintech, China), anti-Integrinβ1 (1:5000, 12594-1-AP, Proteintech, CHN), anti-MRP1 (1:2000, ab260038, Abcam, UK), anti-P-gp (1:1000, 25081-1-AP, Proteintech, China) and anti-GAPDH (1:5000, 10494-1-AP, Proteintech, China). .. The following day, the membrane was incubated with the horseradish peroxidase (HRP)- conjugated secondary antibody (1:2000, ab288151, Abcam, UK) at 37 °C for 90 min.

    Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro.
    Article Snippet: .. Then, the following primary antibodies were added and incubated overnight at 4°C: anti-FGL1 (1:500, 16000-1-AP, Proteintech, China), anti-Integrinβ1 (1:5000, 12594-1-AP, Proteintech, CHN), anti-MRP1 (1:2000, ab260038, Abcam, UK), anti-P-gp (1:1000, 25081-1-AP, Proteintech, China) and antiGAPDH (1:5000, 10494-1-AP, Proteintech, China). .. The following day, the membrane was incubated with the horseradish peroxidase (HRP)- conjugated secondary antibody (1:2000, ab288151, Abcam, UK) at 37 °C for 90 min.



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    Effects of cyclic stretching on <t>integrinβ1</t> and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).
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    Image Search Results


    Effects of cyclic stretching on integrinβ1 and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).

    Journal: Micromachines

    Article Title: A Microfluidic-Based Cell-Stretching Culture Device That Allows for Easy Preparation of Slides for Observation with High-Magnification Objective Lenses

    doi: 10.3390/mi16010093

    Figure Lengend Snippet: Effects of cyclic stretching on integrinβ1 and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).

    Article Snippet: For integrinβ1, vinculin, f-actin, and nuclear staining, 0.5% BSA was added with anti-integrinβ1 antibody (0.4 μg/mL; SC-19656, Santa Cruz Biotechnology, Dallas, TX, USA), anti-vinculin antibody (4 μg/mL; 26520-1-AP, Proteintech, Rosemont, IL, USA), and rhodamine phalloidin (1.65 μM; R4159, Thermo Fisher Scientific) and incubated overnight at 4 °C.

    Techniques: Fluorescence, Cell Culture, Microscopy