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rabbit anti-vsvg antibody  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti-vsvg antibody
    Rabbit Anti Vsvg Antibody, supplied by Cell Signaling Technology Inc, 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/product/rabbit+anti-vsvg+antibody/rabbit+anti+vsvg+antibody/pmc12110046-73-28-37
    Average 90 stars, based on 1 article reviews
    rabbit anti-vsvg antibody - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Saline:

    Article Title: The N-Linked Glycosylation Site N201 in eel Lutropin/Choriogonadotropin Receptor Is Uniquely Indispensable for cAMP Responsiveness and Receptor Surface Loss, but Not pERK1/2 Activity
    Article Snippet: The cells were then washed with Dulbecco’s phosphate-buffered saline (PBS) and fixed with 4% paraformaldehyde for 5 min. After blocking for 30 min, the cells were incubated with rabbit anti-VSVG antibody (1:1000) and horseradish-peroxidase-conjugated anti-rabbit antibody (1:4000) (Cell Signaling Technology, Danvers, MA, USA) for 1 h. Finally, ELISA Femto Maximum Substrate and Luminol/Enhancer were added, and the luminescence signal was measured using a Cytation 3 plate reader.

    Blocking Assay:

    Article Title: The N-Linked Glycosylation Site N201 in eel Lutropin/Choriogonadotropin Receptor Is Uniquely Indispensable for cAMP Responsiveness and Receptor Surface Loss, but Not pERK1/2 Activity
    Article Snippet: The cells were then washed with Dulbecco’s phosphate-buffered saline (PBS) and fixed with 4% paraformaldehyde for 5 min. After blocking for 30 min, the cells were incubated with rabbit anti-VSVG antibody (1:1000) and horseradish-peroxidase-conjugated anti-rabbit antibody (1:4000) (Cell Signaling Technology, Danvers, MA, USA) for 1 h. Finally, ELISA Femto Maximum Substrate and Luminol/Enhancer were added, and the luminescence signal was measured using a Cytation 3 plate reader.

    Incubation:

    Article Title: The N-Linked Glycosylation Site N201 in eel Lutropin/Choriogonadotropin Receptor Is Uniquely Indispensable for cAMP Responsiveness and Receptor Surface Loss, but Not pERK1/2 Activity
    Article Snippet: The cells were then washed with Dulbecco’s phosphate-buffered saline (PBS) and fixed with 4% paraformaldehyde for 5 min. After blocking for 30 min, the cells were incubated with rabbit anti-VSVG antibody (1:1000) and horseradish-peroxidase-conjugated anti-rabbit antibody (1:4000) (Cell Signaling Technology, Danvers, MA, USA) for 1 h. Finally, ELISA Femto Maximum Substrate and Luminol/Enhancer were added, and the luminescence signal was measured using a Cytation 3 plate reader.

    Enzyme-linked Immunosorbent Assay:

    Article Title: The N-Linked Glycosylation Site N201 in eel Lutropin/Choriogonadotropin Receptor Is Uniquely Indispensable for cAMP Responsiveness and Receptor Surface Loss, but Not pERK1/2 Activity
    Article Snippet: The cells were then washed with Dulbecco’s phosphate-buffered saline (PBS) and fixed with 4% paraformaldehyde for 5 min. After blocking for 30 min, the cells were incubated with rabbit anti-VSVG antibody (1:1000) and horseradish-peroxidase-conjugated anti-rabbit antibody (1:4000) (Cell Signaling Technology, Danvers, MA, USA) for 1 h. Finally, ELISA Femto Maximum Substrate and Luminol/Enhancer were added, and the luminescence signal was measured using a Cytation 3 plate reader.



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    (A) Animal cap cells show uniform distribution of injected <t>VSVG-lrp6</t> (VSVG-LRP6; 2 ng). In Activin-treated caps the staining of VSVG-Lrp6 is polarized. (B) DMZ explants from VSVG-Lrp6-injected embryos show preferential localization of Lrp6 at the posterior cell edge. High magnification views of cells in the DMZ are shown in the bottom panels. Injection of myristoylated, plasma membrane localized GFP (mGFP; 500 pg) or anti-actin staining was performed as controls for animal cap and DMZ experiments, respectively. Explants are outlined with solid lines to make their borders readily identifiable. (C) Lrp6 is adjacent to actin-rich regions of cellular extensions. DMZ cells injected with VSVG-Lrp6 were dissociated, plated on fibronectin, immediately fixed, and stained with anti-VSVG (green) and phalloidin (red). Scale bars: animal caps, 30 μm; DMZ (40×), 200 μm; high-magnification DMZ (75×), 50 μm; dissociated cells (200×), 20 μm; high-magnification dissociated cells (350×), 5 μm.
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    Image Search Results


    (A) Animal cap cells show uniform distribution of injected VSVG-lrp6 (VSVG-LRP6; 2 ng). In Activin-treated caps the staining of VSVG-Lrp6 is polarized. (B) DMZ explants from VSVG-Lrp6-injected embryos show preferential localization of Lrp6 at the posterior cell edge. High magnification views of cells in the DMZ are shown in the bottom panels. Injection of myristoylated, plasma membrane localized GFP (mGFP; 500 pg) or anti-actin staining was performed as controls for animal cap and DMZ experiments, respectively. Explants are outlined with solid lines to make their borders readily identifiable. (C) Lrp6 is adjacent to actin-rich regions of cellular extensions. DMZ cells injected with VSVG-Lrp6 were dissociated, plated on fibronectin, immediately fixed, and stained with anti-VSVG (green) and phalloidin (red). Scale bars: animal caps, 30 μm; DMZ (40×), 200 μm; high-magnification DMZ (75×), 50 μm; dissociated cells (200×), 20 μm; high-magnification dissociated cells (350×), 5 μm.

    Journal: Development (Cambridge, England)

    Article Title: Lrp6 is required for convergent extension during Xenopus gastrulation

    doi: 10.1242/dev.010272

    Figure Lengend Snippet: (A) Animal cap cells show uniform distribution of injected VSVG-lrp6 (VSVG-LRP6; 2 ng). In Activin-treated caps the staining of VSVG-Lrp6 is polarized. (B) DMZ explants from VSVG-Lrp6-injected embryos show preferential localization of Lrp6 at the posterior cell edge. High magnification views of cells in the DMZ are shown in the bottom panels. Injection of myristoylated, plasma membrane localized GFP (mGFP; 500 pg) or anti-actin staining was performed as controls for animal cap and DMZ experiments, respectively. Explants are outlined with solid lines to make their borders readily identifiable. (C) Lrp6 is adjacent to actin-rich regions of cellular extensions. DMZ cells injected with VSVG-Lrp6 were dissociated, plated on fibronectin, immediately fixed, and stained with anti-VSVG (green) and phalloidin (red). Scale bars: animal caps, 30 μm; DMZ (40×), 200 μm; high-magnification DMZ (75×), 50 μm; dissociated cells (200×), 20 μm; high-magnification dissociated cells (350×), 5 μm.

    Article Snippet: Antibodies were obtained as follows: rabbit anti-VSVG (Bethyl Laboratories, Montgomery, TX, USA); mouse anti-actin (MP Biomedicals, Solon, OH, USA); Cy2-and Cy3-conjugated secondary antibodies (Jackson Immunoresearch, West Grove, PA, USA).

    Techniques: Injection, Staining