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yap1 polyclonal igg antibody  (Proteintech)


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    Proteintech yap1 polyclonal igg antibody
    Yap1 Polyclonal Igg Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 479 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/yap1+polyclonal+igg+antibody/YAP1+Antibody/pm41537875-221-24-29
    Average 96 stars, based on 479 article reviews
    yap1 polyclonal igg antibody - by Bioz Stars, 2026-10
    96/100 stars

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    Article Title: Packing-driven mechanotransduction: local crowding overrides adhesion and stiffness cues for YAP activation in cellular collectives.
    Article Snippet: The regulation of mechanotransduction is crucial for various cellular processes, including stem cell differentiation, wound healing and cancer progression.. While the activation of mechanotransduction has been extensively studied in single cells, it remains unclear whether similar mechanisms extend to mechanotransduction in multicellular collectives.. Here, by focusing on Yes‐associated protein (YAP), known as the master regulator of mechanotransduction, we reveal that the local packing fraction of cells acts as the primary determinant of YAP activation in cell collectives.

    Article Title: Packing-Driven Mechanotransduction: local crowding overrides adhesion and stiffness cues for YAP Activation in Cellular Collectives
    Article Snippet: .. Cells were immunostained with primary antibodies (mouse-anti YAP monoclonal IgG2a antibody (sc-101199; Santa Cruz biotechnology) (1:400) or the combination of rabbit-anti YAP1 polyclonal IgG antibody (13584-1-AP; ProteinTech) (1:250) and rat-anti E-cadherin Mono-clonal IgG2a Antibody (ECCD-2) (131900 F; ThermoFisher Scientific) (1:250)) in 1% BSA in PBS and incubated at 4°C overnight or for 3 hours at RT (room temperature). .. Cells were washed three times with PBS and incubated for 2 h at RT in secondary antibodies (goat anti-mouse Alexa 568-conjugated IgG antibody (11004) or the combination of Goat anti-Rabbit 568 568-conjugated IgG antibody (A11011) and Goat anti-Rat 568 568-conjugated IgG antibody (A11006) (Life Technologies Corporation)), Alexa Fluor 488 Phalloidin (Invitrogen) (1:500) and nuclear dye Hoechst 350 (33342 Solution; Thermo Fisher Scientific) (1:4,000).



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    KEY RESOURCES TABLE
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    Categorization of LSCC patients and statistical analysis of their correlations with the expression levels of miR-506 and YAP1.

    Journal: Cancer Biology & Therapy

    Article Title: miR-506 is a YAP1-dependent tumor suppressor in laryngeal squamous cell carcinoma

    doi: 10.1080/15384047.2018.1564569

    Figure Lengend Snippet: Categorization of LSCC patients and statistical analysis of their correlations with the expression levels of miR-506 and YAP1.

    Article Snippet: Then, the sections were incubated with the rabbit polyclonal antibody against YAP1 (Cell Signaling Technology, USA) at 4°C overnight.

    Techniques: Expressing

    Correlations between miR-506 and Yap1 in LSCC patients.

    Journal: Cancer Biology & Therapy

    Article Title: miR-506 is a YAP1-dependent tumor suppressor in laryngeal squamous cell carcinoma

    doi: 10.1080/15384047.2018.1564569

    Figure Lengend Snippet: Correlations between miR-506 and Yap1 in LSCC patients.

    Article Snippet: Then, the sections were incubated with the rabbit polyclonal antibody against YAP1 (Cell Signaling Technology, USA) at 4°C overnight.

    Techniques: Expressing

    KEY RESOURCES TABLE

    Journal: Cancer cell

    Article Title: Overcoming Resistance to Dual Innate Immune and MEK Inhibition Downstream of KRAS

    doi: 10.1016/j.ccell.2018.08.009

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Cells were then blocked and permeabilized with 1% BSA and 0.3% Triton X-100 in PBS for 1 hour at room temperature, and incubated with rabbit polyclonal anti-YAP1 (Cell signaling technologies).

    Techniques: Control, Recombinant, Enzyme-linked Immunosorbent Assay, Cell Viability Assay, shRNA, Negative Control, Software, Binding Assay, Expressing