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mouse mab against the v5 tag r960cus antibody  (Thermo Fisher)


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    Thermo Fisher mouse mab against the v5 tag r960cus antibody
    Mouse Mab Against The V5 Tag R960cus Antibody, supplied by Thermo Fisher, 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/mouse mab against the v5 tag r960cus antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    mouse mab against the v5 tag r960cus antibody - by Bioz Stars, 2026-02
    90/100 stars

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    A Cellular thermal shift assay in VTC-037 GSC lysates was used to determine JM2 and JM2-scrambled selective target engagement potency for α-tubulin and β-tubulin. VTC-037 GSC lysates were subjected to different concentration of JM2 or JM2-scrambled (JM2-scrbl) at 57 °C, and peptide affinity was analyzed by western blotting <t>using</t> <t>antibodies</t> against α-tubulin, β-tubulin, and β-actin as negative control. B Percentage of stabilized α-tubulin and β-tubulin at 57 °C was represented, and EC50 values for JM2 and JM2-scrambled (JM2-scrbl) were calculated. C STORM derived point-cloud localizations of Cx43 (green) and α-tubulin (magenta) in VTC-037 GSCs following treatment with JM2-scrambled (JM2-scrbl) or JM2 at 50 μM for 24 h. Zoomed out panels (left) scale bar: 6 μm. Zoomed in panels (middle) scale bar: 1 μm. Zoomed in panels (right) scale bar: 1 μm. Sphere size: 50 nm. D Cross-Pair correlation functions for Cx43/α-tubulin interaction in C ( n = 10). E VTC-037 GSCs were treated or not with antennapedia (ant), JM2, or JM2-scrambled (JM2-scrbl) at 50 μM for 24 h. Following cross-linking, cell lysates were subjected to co-immunoprecipitation using α-tubulin antibody, or <t>V5</t> antibody for negative control, and immunoblotted using antibodies against Cx43, α-tubulin, and GAPDH for loading control. Neutravidin-HRP was used to detect biotin-tagged peptides. HC heavy chain, LC light chain.
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    A Cellular thermal shift assay in VTC-037 GSC lysates was used to determine JM2 and JM2-scrambled selective target engagement potency for α-tubulin and β-tubulin. VTC-037 GSC lysates were subjected to different concentration of JM2 or JM2-scrambled (JM2-scrbl) at 57 °C, and peptide affinity was analyzed by western blotting <t>using</t> <t>antibodies</t> against α-tubulin, β-tubulin, and β-actin as negative control. B Percentage of stabilized α-tubulin and β-tubulin at 57 °C was represented, and EC50 values for JM2 and JM2-scrambled (JM2-scrbl) were calculated. C STORM derived point-cloud localizations of Cx43 (green) and α-tubulin (magenta) in VTC-037 GSCs following treatment with JM2-scrambled (JM2-scrbl) or JM2 at 50 μM for 24 h. Zoomed out panels (left) scale bar: 6 μm. Zoomed in panels (middle) scale bar: 1 μm. Zoomed in panels (right) scale bar: 1 μm. Sphere size: 50 nm. D Cross-Pair correlation functions for Cx43/α-tubulin interaction in C ( n = 10). E VTC-037 GSCs were treated or not with antennapedia (ant), JM2, or JM2-scrambled (JM2-scrbl) at 50 μM for 24 h. Following cross-linking, cell lysates were subjected to co-immunoprecipitation using α-tubulin antibody, or <t>V5</t> antibody for negative control, and immunoblotted using antibodies against Cx43, α-tubulin, and GAPDH for loading control. Neutravidin-HRP was used to detect biotin-tagged peptides. HC heavy chain, LC light chain.
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    ( A ) Immunoblot of whole cell lysate from HEK293T sgNT and sgAKAP11 and sgAKAP11 cells stably expressing the indicated <t>V5-AKAP11</t> construct in triplicate. Cells were grown in DMEM + 10% dFBS. These samples were used for phosphoproteomic experiments. ( B ) Western blots of sgRIα lysates used in Kemptide kinase assay <t>showing</t> <t>vinculin</t> as a loading control and transient expression of FLAG-RIα rescue constructs.
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    A Cellular thermal shift assay in VTC-037 GSC lysates was used to determine JM2 and JM2-scrambled selective target engagement potency for α-tubulin and β-tubulin. VTC-037 GSC lysates were subjected to different concentration of JM2 or JM2-scrambled (JM2-scrbl) at 57 °C, and peptide affinity was analyzed by western blotting using antibodies against α-tubulin, β-tubulin, and β-actin as negative control. B Percentage of stabilized α-tubulin and β-tubulin at 57 °C was represented, and EC50 values for JM2 and JM2-scrambled (JM2-scrbl) were calculated. C STORM derived point-cloud localizations of Cx43 (green) and α-tubulin (magenta) in VTC-037 GSCs following treatment with JM2-scrambled (JM2-scrbl) or JM2 at 50 μM for 24 h. Zoomed out panels (left) scale bar: 6 μm. Zoomed in panels (middle) scale bar: 1 μm. Zoomed in panels (right) scale bar: 1 μm. Sphere size: 50 nm. D Cross-Pair correlation functions for Cx43/α-tubulin interaction in C ( n = 10). E VTC-037 GSCs were treated or not with antennapedia (ant), JM2, or JM2-scrambled (JM2-scrbl) at 50 μM for 24 h. Following cross-linking, cell lysates were subjected to co-immunoprecipitation using α-tubulin antibody, or V5 antibody for negative control, and immunoblotted using antibodies against Cx43, α-tubulin, and GAPDH for loading control. Neutravidin-HRP was used to detect biotin-tagged peptides. HC heavy chain, LC light chain.

    Journal: Cell Death & Disease

    Article Title: Cytoplasmic connexin43-microtubule interactions promote glioblastoma stem-like cell maintenance and tumorigenicity

    doi: 10.1038/s41419-025-07514-2

    Figure Lengend Snippet: A Cellular thermal shift assay in VTC-037 GSC lysates was used to determine JM2 and JM2-scrambled selective target engagement potency for α-tubulin and β-tubulin. VTC-037 GSC lysates were subjected to different concentration of JM2 or JM2-scrambled (JM2-scrbl) at 57 °C, and peptide affinity was analyzed by western blotting using antibodies against α-tubulin, β-tubulin, and β-actin as negative control. B Percentage of stabilized α-tubulin and β-tubulin at 57 °C was represented, and EC50 values for JM2 and JM2-scrambled (JM2-scrbl) were calculated. C STORM derived point-cloud localizations of Cx43 (green) and α-tubulin (magenta) in VTC-037 GSCs following treatment with JM2-scrambled (JM2-scrbl) or JM2 at 50 μM for 24 h. Zoomed out panels (left) scale bar: 6 μm. Zoomed in panels (middle) scale bar: 1 μm. Zoomed in panels (right) scale bar: 1 μm. Sphere size: 50 nm. D Cross-Pair correlation functions for Cx43/α-tubulin interaction in C ( n = 10). E VTC-037 GSCs were treated or not with antennapedia (ant), JM2, or JM2-scrambled (JM2-scrbl) at 50 μM for 24 h. Following cross-linking, cell lysates were subjected to co-immunoprecipitation using α-tubulin antibody, or V5 antibody for negative control, and immunoblotted using antibodies against Cx43, α-tubulin, and GAPDH for loading control. Neutravidin-HRP was used to detect biotin-tagged peptides. HC heavy chain, LC light chain.

    Article Snippet: Mouse-IgG (R&D SystemsTM; MAB002), mouse antibodies against HA.11 tag (Biolegend; 901513), or V5 tag (Cell Signaling Technology; 80076) were used as isotype negative controls.

    Techniques: Thermal Shift Assay, Drug discovery, Concentration Assay, Western Blot, Negative Control, Derivative Assay, Immunoprecipitation, Control

    ( A ) Immunoblot of whole cell lysate from HEK293T sgNT and sgAKAP11 and sgAKAP11 cells stably expressing the indicated V5-AKAP11 construct in triplicate. Cells were grown in DMEM + 10% dFBS. These samples were used for phosphoproteomic experiments. ( B ) Western blots of sgRIα lysates used in Kemptide kinase assay showing vinculin as a loading control and transient expression of FLAG-RIα rescue constructs.

    Journal: The EMBO Journal

    Article Title: Autophagosomes anchor an AKAP11-dependent regulatory checkpoint that shapes neuronal PKA signaling

    doi: 10.1038/s44318-025-00436-x

    Figure Lengend Snippet: ( A ) Immunoblot of whole cell lysate from HEK293T sgNT and sgAKAP11 and sgAKAP11 cells stably expressing the indicated V5-AKAP11 construct in triplicate. Cells were grown in DMEM + 10% dFBS. These samples were used for phosphoproteomic experiments. ( B ) Western blots of sgRIα lysates used in Kemptide kinase assay showing vinculin as a loading control and transient expression of FLAG-RIα rescue constructs.

    Article Snippet: FLAG (#14793), HA (#3724) PKA RI-α (D54D9) (#5675), PKA C-α (D38C6) (#5842), LC3B (D11) (#3868), Vinculin (E1E9V) (#13901), TAX1BP1 (D1D5)(#13901), V5 rabbit (#13202), V5 mouse (#80076), SQSTM1/p62 (#397749), PP2AA (#2041), HOP (#5670), eEF1A (#2551), CACYBP (#3354), HSP90 (#4874), CCT2 (#3561), PSMA2 (#11864), PP2AC (#2259), GPI (#57893), GSK3 β (#12456), Synapsin (#4297), Oct4 (#27505) from Cell Signaling Technologies.

    Techniques: Western Blot, Stable Transfection, Expressing, Construct, Kinase Assay, Control