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lc3 5f10 cleaved caspase 3 asp175 cell signaling technology  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc lc3 5f10 cleaved caspase 3 asp175 cell signaling technology
    Lc3 5f10 Cleaved Caspase 3 Asp175 Cell Signaling Technology, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 17123 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lc3 5f10 cleaved caspase 3 asp175 cell signaling technology/product/Cell Signaling Technology Inc
    Average 99 stars, based on 17123 article reviews
    lc3 5f10 cleaved caspase 3 asp175 cell signaling technology - by Bioz Stars, 2026-06
    99/100 stars

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    90
    Thermo Fisher anti-pmca antibody 5f10
    Expression of <t>PMCA</t> in homogenates from astrocyte (U251 cell line) cultures. ( A ) Twenty-microgram homogenates from U251 cells untreated (C) or treated (A1-like astrocytes) with TNF-α (30 ng/mL), IL-1α (3 ng/mL) and C1q (400 ng/mL), were loaded onto a 10% SDS-polyacrylamide gel, electrotransferred to a PVDF membrane, and immunostained with the PMCA antibody <t>5F10.</t> The anti-GAPDH antibody was used as a protein loading control. ( B ) Quantification of PMCA protein levels in Control and A1-like astrocytes relative to GAPDH is shown as mean ± SEM values, in arbitrary units. Statistical analysis was carried out using the Student’s t -test. (*) p < 0.05 with respect to each Control.
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    Expression of PMCA in homogenates from astrocyte (U251 cell line) cultures. ( A ) Twenty-microgram homogenates from U251 cells untreated (C) or treated (A1-like astrocytes) with TNF-α (30 ng/mL), IL-1α (3 ng/mL) and C1q (400 ng/mL), were loaded onto a 10% SDS-polyacrylamide gel, electrotransferred to a PVDF membrane, and immunostained with the PMCA antibody 5F10. The anti-GAPDH antibody was used as a protein loading control. ( B ) Quantification of PMCA protein levels in Control and A1-like astrocytes relative to GAPDH is shown as mean ± SEM values, in arbitrary units. Statistical analysis was carried out using the Student’s t -test. (*) p < 0.05 with respect to each Control.

    Journal: Molecules

    Article Title: Store-Operated Calcium Entry Inhibition and Plasma Membrane Calcium Pump Upregulation Contribute to the Maintenance of Resting Cytosolic Calcium Concentration in A1-like Astrocytes

    doi: 10.3390/molecules28145363

    Figure Lengend Snippet: Expression of PMCA in homogenates from astrocyte (U251 cell line) cultures. ( A ) Twenty-microgram homogenates from U251 cells untreated (C) or treated (A1-like astrocytes) with TNF-α (30 ng/mL), IL-1α (3 ng/mL) and C1q (400 ng/mL), were loaded onto a 10% SDS-polyacrylamide gel, electrotransferred to a PVDF membrane, and immunostained with the PMCA antibody 5F10. The anti-GAPDH antibody was used as a protein loading control. ( B ) Quantification of PMCA protein levels in Control and A1-like astrocytes relative to GAPDH is shown as mean ± SEM values, in arbitrary units. Statistical analysis was carried out using the Student’s t -test. (*) p < 0.05 with respect to each Control.

    Article Snippet: The primary anti-PMCA antibody (clone 5F10) was purchased from Invitrogen.

    Techniques: Expressing