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Absolute Biotech Inc mouse anti-vsv indiana g antibody
Mouse Anti Vsv Indiana G Antibody, supplied by Absolute Biotech 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/result/mouse anti-vsv indiana g antibody/product/Absolute Biotech Inc
Average 90 stars, based on 1 article reviews
mouse anti-vsv indiana g antibody - by Bioz Stars, 2026-05
90/100 stars

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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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(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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(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