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anti-integrin β1 (p5d2) sc-13590  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology anti-integrin β1 (p5d2) sc-13590
    Anti Integrin β1 (P5d2) Sc 13590, 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/result/anti-integrin β1 (p5d2) sc-13590/product/Santa Cruz Biotechnology
    Average 90 stars, based on 1 article reviews
    anti-integrin β1 (p5d2) sc-13590 - by Bioz Stars, 2026-03
    90/100 stars

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    Figure 4. Laminin density defines RPE mechanical balance via integrin β4/β1 ratio.

    Journal: EMBO reports

    Article Title: Laminin-defined mechanical status modulates retinal pigment epithelium phagocytosis.

    doi: 10.1038/s44319-025-00475-9

    Figure Lengend Snippet: Figure 4. Laminin density defines RPE mechanical balance via integrin β4/β1 ratio.

    Article Snippet: The following azide-free blocking antibodies were used: integrin β1 (clone P5D2) (Santa Cruz, sc-13590 L), integrin β4 (clone ASC-8) (Merk, MAB2059Z), integrin αvβ3 (clone LM609) (Merk, MAB1976Z), integrin α3 (clone P1B5) (Merk, MAB1952Z), integrin α5 (clone P1D6) (Merk, MAB1956Z), integrin α6 (clone GOH3) (Santa Cruz, sc-19622 L).

    Techniques:

    Figure 10. (A,B) Representative confocal microscopy analysis of F-actin (Red) and integrin-β1 (green) distribution in MDA-MB-231 cells cultured under control conditions or treated with ZFEs for 96 h. Control cells exhibited a dense network of stress fibers (A). After ZFEs treatment, F-actin began to reorganize along the cell membrane, with lamellipodia and filopodia being nearly absent (B). Scale bars: 10 µm. (C,D) Representative confocal microscopy analysis of β-catenin (red) and E- cadherin (green) distribution in MDA-MB-231 cells cultured in control conditions or treated with ZFEs for 96 h. In untreated MDA-MB-231 cells, β-catenin was primarily localized in the cytosol and E-cadherin was completely absent (C). ZFEs treatment promoted the accumulation of β-catenin/E- cadherin complexes at the cell membrane, facilitating cell-to-cell contact and the reconstitution of an epithelial-like architecture (D). Scale bars: 20 µm.

    Journal: International Journal of Molecular Sciences

    Article Title: miRNAs from Zebrafish Embryo Extracts Inhibit Breast Cancer Invasiveness and Migration by Modulating miR-218-5p/PI3K Pathway

    doi: 10.3390/ijms26083812

    Figure Lengend Snippet: Figure 10. (A,B) Representative confocal microscopy analysis of F-actin (Red) and integrin-β1 (green) distribution in MDA-MB-231 cells cultured under control conditions or treated with ZFEs for 96 h. Control cells exhibited a dense network of stress fibers (A). After ZFEs treatment, F-actin began to reorganize along the cell membrane, with lamellipodia and filopodia being nearly absent (B). Scale bars: 10 µm. (C,D) Representative confocal microscopy analysis of β-catenin (red) and E- cadherin (green) distribution in MDA-MB-231 cells cultured in control conditions or treated with ZFEs for 96 h. In untreated MDA-MB-231 cells, β-catenin was primarily localized in the cytosol and E-cadherin was completely absent (C). ZFEs treatment promoted the accumulation of β-catenin/E- cadherin complexes at the cell membrane, facilitating cell-to-cell contact and the reconstitution of an epithelial-like architecture (D). Scale bars: 20 µm.

    Article Snippet: Finally, anti-integrin β1 antibody (sc8978 Santa Cruz, Dallas, TX, USA) was used with the secondary antibody goat anti-rabbit IgG Alexa Fluor® 488 (A11008; Invitrogen, Carlsbad, CA, USA) and Phalloidin TRITC labeled (P1951 Sigma-Aldrich–M.

    Techniques: Confocal Microscopy, Cell Culture, Control, Membrane