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mouse monoclonal primary anti serca antibody  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology mouse monoclonal primary anti serca antibody
    Mouse Monoclonal Primary Anti Serca Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 340 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/monoclonal+serca2+antibody/SERCA2+Antibody/pm41369381-58-7-12
    Average 94 stars, based on 340 article reviews
    mouse monoclonal primary anti serca antibody - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Incubation:

    Article Title: Redox Regulation of SERCA2 Is Required for Vascular Endothelial Growth Factor-Induced Signaling and Endothelial Cell Migration
    Article Snippet: .. Cells were treated with VEGF for 5 min or • NO gas solution (10 μ M ) for 1 min. Lysates were incubated with a custom polyclonal SERCA2 antibody and immunoblotted with a monoclonal GSH antibody (Virogen) and a monoclonal SERCA2 antibody (Santa Cruz). .. HAECs plated on gelatin-coated glass coverslips were loaded with 2 μM Fura2-AM (Invitrogen) in the presence of 0.02% pluronic F127 (Invitrogen) in serum-free endothelial growth media, and right before the experiment were transferred to nominally Ca 2+ -free PSS supplemented with 2.5 mM probenecid (Alfa Aesar, Ward Hill, MA).



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    FBS-induced RyR2 ablation underlies impaired Wnt responsiveness in AC16 cells. ( A and B ) Cytosol and SR calcium levels of AC16 cells preincubated with H 2 O or CHX (1 μg/ml) for 15 min before treatment with Wnt modulators for 6 h. Error bars indicate SD ( n = 6). ( C and E ) Western blot analysis of RyR2 and <t>SERCA2a</t> levels in AC16 cells in the medium with or without FBS treated with SFRP2 (10 μg/ml) or LiCl (20 mM) for 6 h. Error bars indicate SD ( n = 3). ( D and F ) Relative RyR2 and SERCA2a mRNA levels in AC16 cells with or without FBS treated with SFRP2 or LiCl for 6 h. Error bars indicate SD ( n = 6). ( G ) Relative RyR2 mRNA level for ‘RyR2-reconstituted’ cells compared to AC16 cells without FBS. ( H and I ) Cytosol and SR calcium levels of AC16 cells in FBS medium (labeled ‘Without RyR2’) and ‘RyR2-reconstituted’ cells in FBS medium (labeled ‘With RyR2’). ( J and K ) Cytosol and SR calcium levels of ‘RyR2-reconstituted’ cells in FBS medium and AC16 cells without FBS. Error bars indicate SD ( n = 6).
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    Image Search Results


    FBS-induced RyR2 ablation underlies impaired Wnt responsiveness in AC16 cells. ( A and B ) Cytosol and SR calcium levels of AC16 cells preincubated with H 2 O or CHX (1 μg/ml) for 15 min before treatment with Wnt modulators for 6 h. Error bars indicate SD ( n = 6). ( C and E ) Western blot analysis of RyR2 and SERCA2a levels in AC16 cells in the medium with or without FBS treated with SFRP2 (10 μg/ml) or LiCl (20 mM) for 6 h. Error bars indicate SD ( n = 3). ( D and F ) Relative RyR2 and SERCA2a mRNA levels in AC16 cells with or without FBS treated with SFRP2 or LiCl for 6 h. Error bars indicate SD ( n = 6). ( G ) Relative RyR2 mRNA level for ‘RyR2-reconstituted’ cells compared to AC16 cells without FBS. ( H and I ) Cytosol and SR calcium levels of AC16 cells in FBS medium (labeled ‘Without RyR2’) and ‘RyR2-reconstituted’ cells in FBS medium (labeled ‘With RyR2’). ( J and K ) Cytosol and SR calcium levels of ‘RyR2-reconstituted’ cells in FBS medium and AC16 cells without FBS. Error bars indicate SD ( n = 6).

    Journal: Journal of Molecular Cell Biology

    Article Title: Canonical Wnt signaling affects calcium homeostasis in serum-treated AC16 cells through MLN-mediated SERCA2a regulation

    doi: 10.1093/jmcb/mjaf050

    Figure Lengend Snippet: FBS-induced RyR2 ablation underlies impaired Wnt responsiveness in AC16 cells. ( A and B ) Cytosol and SR calcium levels of AC16 cells preincubated with H 2 O or CHX (1 μg/ml) for 15 min before treatment with Wnt modulators for 6 h. Error bars indicate SD ( n = 6). ( C and E ) Western blot analysis of RyR2 and SERCA2a levels in AC16 cells in the medium with or without FBS treated with SFRP2 (10 μg/ml) or LiCl (20 mM) for 6 h. Error bars indicate SD ( n = 3). ( D and F ) Relative RyR2 and SERCA2a mRNA levels in AC16 cells with or without FBS treated with SFRP2 or LiCl for 6 h. Error bars indicate SD ( n = 6). ( G ) Relative RyR2 mRNA level for ‘RyR2-reconstituted’ cells compared to AC16 cells without FBS. ( H and I ) Cytosol and SR calcium levels of AC16 cells in FBS medium (labeled ‘Without RyR2’) and ‘RyR2-reconstituted’ cells in FBS medium (labeled ‘With RyR2’). ( J and K ) Cytosol and SR calcium levels of ‘RyR2-reconstituted’ cells in FBS medium and AC16 cells without FBS. Error bars indicate SD ( n = 6).

    Article Snippet: Monoclonal anti-SERCA2a antibody (ABclonal, A11692), monoclonal anti-RyR2 (Abcam, ab224803), polyclonal anti-MLN (Thermofisher, MYREGLN-101AP), monoclonal anti-tubulin antibody (Abcam, ab7291), and monoclonal anti-GAPDH (Abcam, ab8245) were used.

    Techniques: Western Blot, Labeling

    Wnt inhibition upregulates MLN expression to suppress SERCA2a activity. ( A ) Relative SERCA2a activity in AC16 cells in FBS medium. ( B ) Gene expression of known SERCA2a modulators in AC16 cells with or without FBS treated with different Wnt modulators (LiCl: 20 mM; SFRP2: 10 μg/ml; XAV939: 10 μM; LF3: 1 μM) for 6 h. ( C ) Relative MLN mRNA level in AC16 cells with FBS treatment. ( D ) Western blot analysis of MLN in AC16 cells with FBS treatment. ( E and F ) Cytosol and SR calcium levels of MLN-knockdown cell lines in FBS medium. ( G and H ) Cytosol and SR calcium levels of MLN-kd2 AC16 cells in FBS medium and AC16 cells without FBS. Error bars indicate SD ( n = 6).

    Journal: Journal of Molecular Cell Biology

    Article Title: Canonical Wnt signaling affects calcium homeostasis in serum-treated AC16 cells through MLN-mediated SERCA2a regulation

    doi: 10.1093/jmcb/mjaf050

    Figure Lengend Snippet: Wnt inhibition upregulates MLN expression to suppress SERCA2a activity. ( A ) Relative SERCA2a activity in AC16 cells in FBS medium. ( B ) Gene expression of known SERCA2a modulators in AC16 cells with or without FBS treated with different Wnt modulators (LiCl: 20 mM; SFRP2: 10 μg/ml; XAV939: 10 μM; LF3: 1 μM) for 6 h. ( C ) Relative MLN mRNA level in AC16 cells with FBS treatment. ( D ) Western blot analysis of MLN in AC16 cells with FBS treatment. ( E and F ) Cytosol and SR calcium levels of MLN-knockdown cell lines in FBS medium. ( G and H ) Cytosol and SR calcium levels of MLN-kd2 AC16 cells in FBS medium and AC16 cells without FBS. Error bars indicate SD ( n = 6).

    Article Snippet: Monoclonal anti-SERCA2a antibody (ABclonal, A11692), monoclonal anti-RyR2 (Abcam, ab224803), polyclonal anti-MLN (Thermofisher, MYREGLN-101AP), monoclonal anti-tubulin antibody (Abcam, ab7291), and monoclonal anti-GAPDH (Abcam, ab8245) were used.

    Techniques: Inhibition, Expressing, Activity Assay, Gene Expression, Western Blot, Knockdown

    Combined MLN knockdown and RyR2 overexpression restores canonical Wnt-mediated calcium regulation in FBS-treated AC16 cells. ( A ) Relative SERCA2a activity in FBS-treated AC16 cells and MLN-kd2 cells under various treatments. Cells were treated with the SERCA2a activator SAA (1 μM), the Wnt inhibitor SFRP2 (10 μg/ml), or the SERCA2a inhibitor Tg (100 nM) for 6 h. MLN knockdown significantly increased basal SERCA2a activity and abolished SFRP2-induced suppression. ( B ) Relative SERCA2a activity in MLN-kd2 cells treated with canonical Wnt inhibitors (SFRP2: 10 μg/ml; XAV939: 10 μM; LF3: 1 μM) or the SERCA2a activator SAA (1 μM) for 6 h. ( C and D ) Cytosol and SR calcium levels in modified AC16 cells (‘New AC16 cells’) with combined MLN knockdown and RyR2 overexpression, compared to standard FBS-free AC16 cells and FBS-treated AC16 cells. Cells were treated with the Wnt activator LiCl (20 mM) or the Wnt inhibitor SFRP2 (10 μg/ml) for 6 h. Error bars indicate SD ( n = 6).

    Journal: Journal of Molecular Cell Biology

    Article Title: Canonical Wnt signaling affects calcium homeostasis in serum-treated AC16 cells through MLN-mediated SERCA2a regulation

    doi: 10.1093/jmcb/mjaf050

    Figure Lengend Snippet: Combined MLN knockdown and RyR2 overexpression restores canonical Wnt-mediated calcium regulation in FBS-treated AC16 cells. ( A ) Relative SERCA2a activity in FBS-treated AC16 cells and MLN-kd2 cells under various treatments. Cells were treated with the SERCA2a activator SAA (1 μM), the Wnt inhibitor SFRP2 (10 μg/ml), or the SERCA2a inhibitor Tg (100 nM) for 6 h. MLN knockdown significantly increased basal SERCA2a activity and abolished SFRP2-induced suppression. ( B ) Relative SERCA2a activity in MLN-kd2 cells treated with canonical Wnt inhibitors (SFRP2: 10 μg/ml; XAV939: 10 μM; LF3: 1 μM) or the SERCA2a activator SAA (1 μM) for 6 h. ( C and D ) Cytosol and SR calcium levels in modified AC16 cells (‘New AC16 cells’) with combined MLN knockdown and RyR2 overexpression, compared to standard FBS-free AC16 cells and FBS-treated AC16 cells. Cells were treated with the Wnt activator LiCl (20 mM) or the Wnt inhibitor SFRP2 (10 μg/ml) for 6 h. Error bars indicate SD ( n = 6).

    Article Snippet: Monoclonal anti-SERCA2a antibody (ABclonal, A11692), monoclonal anti-RyR2 (Abcam, ab224803), polyclonal anti-MLN (Thermofisher, MYREGLN-101AP), monoclonal anti-tubulin antibody (Abcam, ab7291), and monoclonal anti-GAPDH (Abcam, ab8245) were used.

    Techniques: Knockdown, Over Expression, Activity Assay, Modification