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mouse anti vsv g  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology mouse anti vsv g
    Mouse Anti Vsv G, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 77 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+vsv+g/VSV-G+Antibody/pmc12891724-485-11-27
    Average 94 stars, based on 77 article reviews
    mouse anti vsv g - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: ARRDC3 promotes lysosome-mediated YAP degradation to inhibit enterovirus replication
    Article Snippet: The primary antibodies used were rabbit anti-YAP (1:2500, ET1608-30, Huabio, China), rabbit anti-ARRDC3 (1:500, 34169, SAB, USA), rabbit anti-HA (1:4000, 51064-2-AP, Proteintech, China), rabbit anti-beta-actin (1:1000, 81115-1-RR, Proteintech, China), mouse anti-EV-D68 VP1 (1:2000, GTX633770, Gene Tex, China), rabbit anti-EV-A71 VP1 (1:2000, GTX132339, Gene Tex, China), rabbit anti-Myc (1:1000, M20002F, Abmart, China), rabbit anti-GAPDH (1:1000, D264398, Sangon, China), goat anti-HPIV3 HN (1:2500, ab28584, Abcam, United Kingdom) and mouse anti-VSV-G (1:1000, sc-365019, Santa Cruz Biotechnology, USA).

    Article Title: Characterization of Endogenous SERINC5 Protein as Anti-HIV-1 Factor
    Article Snippet: Proteins were run on a 10% SDS-PAGE gel and transferred onto nitrocellulose using a semidry transfer system (Biometra).

    Article Title: Use of the chromosome 19 microRNA cluster (C19MC) for treating microbial disease and promoting authophagy
    Article Snippet: Rapamycin (5 μM, Calbiochem) treatment or serum-starvation with Hank's Balanced salt solution (HBSS) for 4 h was used as a positive control for autophagy.

    Article Title: A protein-interaction network of interferon-stimulated genes extends the innate immune system landscape.
    Article Snippet: 1Innate Immunity Laboratory, Max-Planck Institute of Biochemistry, Munich, Germany.. 2Institute of Virology, School of Medicine, Technical University of Munich, Munich, Germany.. 3Laboratory of Virology and Infectious Disease, The Rockefeller University, New York, NY, USA.

    Article Title: Use of the chromosome 19 microRNA cluster (C19MC) for treating viral disease and promoting authophagy
    Article Snippet: Rapamycin (5 μM, Calbiochem) treatment or serum-starvation with Hank's Balanced salt solution (HBSS) for 4 h was used as a positive control for autophagy.

    Virus:

    Article Title: Herpes Simplex Virus and Interferon Signaling Induce Novel Autophagic Clusters in Sensory Neurons
    Article Snippet: .. Primary antibodies used were rabbit anti-β-III-tubulin (Abcam; ab18207), mouse anti-NeuN (Millipore; MAB377), rabbit anti-HSV-1 (Dako; B0114), rabbit anti-MHV-68 (kindly provided by Edward Usherwood), mouse anti-vaccinia virus (Thermo Scientific; MA1-7484), mouse anti-TMEV (kindly provided by Andrew Pachner), mouse anti-YFV (Santa Cruz; 3576), mouse anti-VSV-G (Santa Cruz; P5D4), rabbit anti-β-galactosidase (anti-β-Gal; Rockland; 100-4136), mouse anti-ICP0 (Virusys; H1A027), mouse anti-VP16 (Santa Cruz; 7545), mouse anti-ICP5 (Abcam; ab6508), rabbit anti-LC3 (MBL [PD014] and Cell Signaling [12741]), rabbit anti-p62 (Novus; NBP1-48320), rat anti-LAMP1 (Santa Cruz; 1D4B), rabbit anti-PABP (Abcam; ab21060), goat anti-TIA (Santa Cruz; 1751), rabbit anti-HDAC6 (Assay Biotech; B0941), rabbit anti-γ-tubulin (Bioss; bs-1322R), and rabbit anti-ISG15 (Abgent; AP1150a). .. Secondary antibodies were goat or donkey anti-mouse, -rabbit, or -rat, conjugated to Alexa 405, 488, 555, or 647 (Invitrogen).

    Western Blot:

    Article Title: O -GlcNAcylation of AMFR stabilizes TSPAN4 to regulate migrasome formation for viral release
    Article Snippet: Mouse anti-Tubulin (E7, WB 1:10000) was obtained from Developmental Studies Hybridoma Bank. .. Mouse anti-GAPDH (sc-365062, WB 1:5000), mouse anti-HSV-1/2 ICP27 (SC-69807, WB 1:500), mouse anti-VSV-G (SC-365019, WB 1:500, IF 1:200) and mouse anti-TOM20 (SC-17764, WB 1:500) were obtained from Santa Cruz Biotechnology. .. Mouse anti-VSV-M (EB0011, WB 1:1000) was obtained from Kerafast.

    Incubation:

    Article Title: Characterization of Endogenous SERINC5 Protein as Anti-HIV-1 Factor
    Article Snippet: Proteins were run on a 10% SDS-PAGE gel and transferred onto nitrocellulose using a semidry transfer system (Biometra). .. Blocked membranes were incubated with the following primary antibodies: rabbit anti-mitogen-activated protein kinase (MAPK) (Santa Cruz), mouse anti-HA (clone HA-7; Sigma), mouse anti-p24 (ExBio), rabbit anti-HIV-1 p24CA (ExBio), mouse anti-interferonstimulated gene 15 (ISG15) (clone F-9; Santa Cruz Technologies), and mouse anti-VSV-G (Santa Cruz) (a kind gift from Hanna-Mari Baldauf). .. Secondary antibodies conjugated to Alexa Fluor 680/800 fluorescent dyes were used for detection and quantification with the Odyssey infrared imaging system (Li-Cor Biosciences).



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    (A) Schematic showing production of lentiviruses (LV) from Myomaker- and Myomerger-expressing HEK293T cells. (B) Western blot for Myomaker, Myomerger, and GAPDH on HEK293T cell lysates after various times of doxycycline treatment. (C) Western blot on concentrated viral particles for Myomaker, Myomaker, <t>and</t> <t>VSV-G.</t> (D) Western blot on Bald-LVs and Mymk+Mymg-LVs for viral components and the muscle fusogens. (E) Representative images from transmission electron microscopy on VSV-G-LVs and Mymk+Mymg-LVs. Scale bar, 100 nm. (F) Images from immunogold electron microscopy using the indicated antibodies on the pseudotyped lentiviruses. Myomaker and Myomerger antibodies were detected in the same sample using gold particles of different sizes. Scale bar, 200 nm. (G) Representative images of empty and Mymk+Mymg target cells after application of Bald GFP-encoding LVs or LVs pseudotyped with VSV-G or Myomaker and Myomerger. Nuclei were stained with Hoechst. Scale bar, 100 μm. (H) Quantification of titers for VSV-G-LVs and Mymk+Mymk-LVs prior to concentration of supernatants. Each sample is an average of 3–4 replicates from independent viral preparations. Titers were determined on Mymk+Mymg BHK21 cells. (I) Representative images from cultures of differentiated myotubes, proliferating myoblasts, and fibroblasts that were treated with Bald-LV-GFP or Mymk+Mymg-LV-GFP. Cells were stained with Phalloidin and Hoechst. Scale bar, 100 μm. GFP+ cells were quantified for each cell type and histograms are shown on the right. Data are presented as mean ± standard deviation. Statistical test used was an unpaired t-test with Welch’s correction; ***p<0.001, ****p<0.0001.
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    Cusabio mouse anti v5 tag antibody
    (A) Schematic showing production of lentiviruses (LV) from Myomaker- and Myomerger-expressing HEK293T cells. (B) Western blot for Myomaker, Myomerger, and GAPDH on HEK293T cell lysates after various times of doxycycline treatment. (C) Western blot on concentrated viral particles for Myomaker, Myomaker, <t>and</t> <t>VSV-G.</t> (D) Western blot on Bald-LVs and Mymk+Mymg-LVs for viral components and the muscle fusogens. (E) Representative images from transmission electron microscopy on VSV-G-LVs and Mymk+Mymg-LVs. Scale bar, 100 nm. (F) Images from immunogold electron microscopy using the indicated antibodies on the pseudotyped lentiviruses. Myomaker and Myomerger antibodies were detected in the same sample using gold particles of different sizes. Scale bar, 200 nm. (G) Representative images of empty and Mymk+Mymg target cells after application of Bald GFP-encoding LVs or LVs pseudotyped with VSV-G or Myomaker and Myomerger. Nuclei were stained with Hoechst. Scale bar, 100 μm. (H) Quantification of titers for VSV-G-LVs and Mymk+Mymk-LVs prior to concentration of supernatants. Each sample is an average of 3–4 replicates from independent viral preparations. Titers were determined on Mymk+Mymg BHK21 cells. (I) Representative images from cultures of differentiated myotubes, proliferating myoblasts, and fibroblasts that were treated with Bald-LV-GFP or Mymk+Mymg-LV-GFP. Cells were stained with Phalloidin and Hoechst. Scale bar, 100 μm. GFP+ cells were quantified for each cell type and histograms are shown on the right. Data are presented as mean ± standard deviation. Statistical test used was an unpaired t-test with Welch’s correction; ***p<0.001, ****p<0.0001.
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    Image Search Results


    (A) Schematic showing production of lentiviruses (LV) from Myomaker- and Myomerger-expressing HEK293T cells. (B) Western blot for Myomaker, Myomerger, and GAPDH on HEK293T cell lysates after various times of doxycycline treatment. (C) Western blot on concentrated viral particles for Myomaker, Myomaker, and VSV-G. (D) Western blot on Bald-LVs and Mymk+Mymg-LVs for viral components and the muscle fusogens. (E) Representative images from transmission electron microscopy on VSV-G-LVs and Mymk+Mymg-LVs. Scale bar, 100 nm. (F) Images from immunogold electron microscopy using the indicated antibodies on the pseudotyped lentiviruses. Myomaker and Myomerger antibodies were detected in the same sample using gold particles of different sizes. Scale bar, 200 nm. (G) Representative images of empty and Mymk+Mymg target cells after application of Bald GFP-encoding LVs or LVs pseudotyped with VSV-G or Myomaker and Myomerger. Nuclei were stained with Hoechst. Scale bar, 100 μm. (H) Quantification of titers for VSV-G-LVs and Mymk+Mymk-LVs prior to concentration of supernatants. Each sample is an average of 3–4 replicates from independent viral preparations. Titers were determined on Mymk+Mymg BHK21 cells. (I) Representative images from cultures of differentiated myotubes, proliferating myoblasts, and fibroblasts that were treated with Bald-LV-GFP or Mymk+Mymg-LV-GFP. Cells were stained with Phalloidin and Hoechst. Scale bar, 100 μm. GFP+ cells were quantified for each cell type and histograms are shown on the right. Data are presented as mean ± standard deviation. Statistical test used was an unpaired t-test with Welch’s correction; ***p<0.001, ****p<0.0001.

    Journal: Cell

    Article Title: Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery

    doi: 10.1016/j.cell.2023.03.033

    Figure Lengend Snippet: (A) Schematic showing production of lentiviruses (LV) from Myomaker- and Myomerger-expressing HEK293T cells. (B) Western blot for Myomaker, Myomerger, and GAPDH on HEK293T cell lysates after various times of doxycycline treatment. (C) Western blot on concentrated viral particles for Myomaker, Myomaker, and VSV-G. (D) Western blot on Bald-LVs and Mymk+Mymg-LVs for viral components and the muscle fusogens. (E) Representative images from transmission electron microscopy on VSV-G-LVs and Mymk+Mymg-LVs. Scale bar, 100 nm. (F) Images from immunogold electron microscopy using the indicated antibodies on the pseudotyped lentiviruses. Myomaker and Myomerger antibodies were detected in the same sample using gold particles of different sizes. Scale bar, 200 nm. (G) Representative images of empty and Mymk+Mymg target cells after application of Bald GFP-encoding LVs or LVs pseudotyped with VSV-G or Myomaker and Myomerger. Nuclei were stained with Hoechst. Scale bar, 100 μm. (H) Quantification of titers for VSV-G-LVs and Mymk+Mymk-LVs prior to concentration of supernatants. Each sample is an average of 3–4 replicates from independent viral preparations. Titers were determined on Mymk+Mymg BHK21 cells. (I) Representative images from cultures of differentiated myotubes, proliferating myoblasts, and fibroblasts that were treated with Bald-LV-GFP or Mymk+Mymg-LV-GFP. Cells were stained with Phalloidin and Hoechst. Scale bar, 100 μm. GFP+ cells were quantified for each cell type and histograms are shown on the right. Data are presented as mean ± standard deviation. Statistical test used was an unpaired t-test with Welch’s correction; ***p<0.001, ****p<0.0001.

    Article Snippet: Mouse anti-VSV-G , Kerafast , Cat #8G5F11.

    Techniques: Expressing, Western Blot, Transmission Assay, Electron Microscopy, Staining, Concentration Assay, Standard Deviation

    (A) Top panel displays experimental design for analysis of muscle progenitors. Middle panels show representative FACS plots and quantification for α7-Integrin+ myogenic cells (y-axis) and tdTomato+ cells (x-axis) from mdx4cv; RosatdTom muscle that received Bald-LV-Cre or Mymk+Mymg-LV-Cre. Bottom panels show representative FACS plots and quantification for tdTomato+ non-myogenic interstitial cells. (B) Top panel is the experimental design using lentivirus encoding for luciferase that was pseudotyped with Bald, VSV-G, or Myomaker and Myomerger. After cardiotoxin injury, lentiviruses were injected intramuscularly and bioluminesence measured through IVIS imaging multiple time points after viral delivery. Representative pseudocolored images show a progressive increase in bioluminescence in the muscles treated with Myomaker and Myomerger-pseudotyped virus. Bottom panel is quantification of bioluminescence for muscles transduced with lentivirus containing Myomaker and Myomerger. (C) Mdx4cv; RosatdTom mice received an intramuscular injection of Bald-LV-Cre or Mymk+Mymg-LV-Cre, then 2 weeks later some mice were injured with cardiotoxin. Representative images for tdTomato+ myofibers are shown to the right. Nuclei were stained with DAPI. Scale bar, 100 μm. Bottom, left panel shows quantification of the percentage of tdTomato+ myofibers. Data are presented as mean ± standard deviation; data in (A, B) combined from at least two independent lentiviral preparations; data in (C) is from one lentiviral preparation. Statistical tests used were (A) unpaired t-test with Welch’s correction; (B) Friedman test with Dunn’s correction for multiple comparisons; (C) Two-way ANOVA with Tukey’s correction for multiple comparisons; **p< 0.01, ****p< 0.0001.

    Journal: Cell

    Article Title: Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery

    doi: 10.1016/j.cell.2023.03.033

    Figure Lengend Snippet: (A) Top panel displays experimental design for analysis of muscle progenitors. Middle panels show representative FACS plots and quantification for α7-Integrin+ myogenic cells (y-axis) and tdTomato+ cells (x-axis) from mdx4cv; RosatdTom muscle that received Bald-LV-Cre or Mymk+Mymg-LV-Cre. Bottom panels show representative FACS plots and quantification for tdTomato+ non-myogenic interstitial cells. (B) Top panel is the experimental design using lentivirus encoding for luciferase that was pseudotyped with Bald, VSV-G, or Myomaker and Myomerger. After cardiotoxin injury, lentiviruses were injected intramuscularly and bioluminesence measured through IVIS imaging multiple time points after viral delivery. Representative pseudocolored images show a progressive increase in bioluminescence in the muscles treated with Myomaker and Myomerger-pseudotyped virus. Bottom panel is quantification of bioluminescence for muscles transduced with lentivirus containing Myomaker and Myomerger. (C) Mdx4cv; RosatdTom mice received an intramuscular injection of Bald-LV-Cre or Mymk+Mymg-LV-Cre, then 2 weeks later some mice were injured with cardiotoxin. Representative images for tdTomato+ myofibers are shown to the right. Nuclei were stained with DAPI. Scale bar, 100 μm. Bottom, left panel shows quantification of the percentage of tdTomato+ myofibers. Data are presented as mean ± standard deviation; data in (A, B) combined from at least two independent lentiviral preparations; data in (C) is from one lentiviral preparation. Statistical tests used were (A) unpaired t-test with Welch’s correction; (B) Friedman test with Dunn’s correction for multiple comparisons; (C) Two-way ANOVA with Tukey’s correction for multiple comparisons; **p< 0.01, ****p< 0.0001.

    Article Snippet: Mouse anti-VSV-G , Kerafast , Cat #8G5F11.

    Techniques: Luciferase, Injection, Imaging, Muscles, Virus, Transduction, Staining, Standard Deviation

    KEY RESOURCES TABLE

    Journal: Cell

    Article Title: Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery

    doi: 10.1016/j.cell.2023.03.033

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Mouse anti-VSV-G , Kerafast , Cat #8G5F11.

    Techniques: Virus, Recombinant, Membrane, Plasmid Preparation, Electron Microscopy, Protease Inhibitor, Clone Assay, Modification, Software, Transmission Assay, Microscopy, Inverted Microscopy, In Vivo Imaging