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fluorescent protein gfp reporter  (OriGene)


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    Structured Review

    OriGene fluorescent protein gfp reporter
    (A) Representative <t>fluorescent</t> images of MOC1 and MOC2 cells after 48 h of incubation with increasing titers of <t>GFP-expressing</t> RP1-15. GFP shown in gray scale. (B) MOC1 and MOC2 cell viability after 48 h with increasing RP1 titers in vitro, assessed via CellTiter-Glo assay. Significance determined using 1-way ANOVA with Dunnett test. RLU = relative light units.
    Fluorescent Protein Gfp Reporter, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fluorescent+protein+gfp+reporter/PD-L1+(Cd274)+(NM_021893)+Mouse+Tagged+ORF+Clone/pmc13224917-19-31-37
    Average 94 stars, based on 2 article reviews
    fluorescent protein gfp reporter - by Bioz Stars, 2026-10
    94/100 stars

    Images

    1) Product Images from "PD-L1 Immuno-PET Reveals Systemic Effects of Localized Oncolytic Virotherapy in a Mouse Model of Head and Neck Cancer"

    Article Title: PD-L1 Immuno-PET Reveals Systemic Effects of Localized Oncolytic Virotherapy in a Mouse Model of Head and Neck Cancer

    Journal: Journal of Nuclear Medicine

    doi: 10.2967/jnumed.125.270922

    (A) Representative fluorescent images of MOC1 and MOC2 cells after 48 h of incubation with increasing titers of GFP-expressing RP1-15. GFP shown in gray scale. (B) MOC1 and MOC2 cell viability after 48 h with increasing RP1 titers in vitro, assessed via CellTiter-Glo assay. Significance determined using 1-way ANOVA with Dunnett test. RLU = relative light units.
    Figure Legend Snippet: (A) Representative fluorescent images of MOC1 and MOC2 cells after 48 h of incubation with increasing titers of GFP-expressing RP1-15. GFP shown in gray scale. (B) MOC1 and MOC2 cell viability after 48 h with increasing RP1 titers in vitro, assessed via CellTiter-Glo assay. Significance determined using 1-way ANOVA with Dunnett test. RLU = relative light units.

    Techniques Used: Incubation, Expressing, In Vitro, Glo Assay

    Related Articles

    Generated:

    Article Title: PD-L1 Immuno-PET Reveals Systemic Effects of Localized Oncolytic Virotherapy in a Mouse Model of Head and Neck Cancer
    Article Snippet: .. The MOC2( PD-L1 ) cell line was generated in our laboratory to overexpress PD-L1 by transducing MOC2 cells with a lentiviral vector carrying the murine CD274 gene tagged with a green fluorescent protein (GFP) reporter (MR 203953L2; OriGene Technologies). .. The GFP-positive cell population was isolated using a MoFlo Astrios cell sorter (Beckman Coulter).

    Magnetic Resonance Imaging:

    Article Title: PD-L1 Immuno-PET Reveals Systemic Effects of Localized Oncolytic Virotherapy in a Mouse Model of Head and Neck Cancer
    Article Snippet: .. The MOC2( PD-L1 ) cell line was generated in our laboratory to overexpress PD-L1 by transducing MOC2 cells with a lentiviral vector carrying the murine CD274 gene tagged with a green fluorescent protein (GFP) reporter (MR 203953L2; OriGene Technologies). .. The GFP-positive cell population was isolated using a MoFlo Astrios cell sorter (Beckman Coulter).



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    Image Search Results


    (A) Representative fluorescent images of MOC1 and MOC2 cells after 48 h of incubation with increasing titers of GFP-expressing RP1-15. GFP shown in gray scale. (B) MOC1 and MOC2 cell viability after 48 h with increasing RP1 titers in vitro, assessed via CellTiter-Glo assay. Significance determined using 1-way ANOVA with Dunnett test. RLU = relative light units.

    Journal: Journal of Nuclear Medicine

    Article Title: PD-L1 Immuno-PET Reveals Systemic Effects of Localized Oncolytic Virotherapy in a Mouse Model of Head and Neck Cancer

    doi: 10.2967/jnumed.125.270922

    Figure Lengend Snippet: (A) Representative fluorescent images of MOC1 and MOC2 cells after 48 h of incubation with increasing titers of GFP-expressing RP1-15. GFP shown in gray scale. (B) MOC1 and MOC2 cell viability after 48 h with increasing RP1 titers in vitro, assessed via CellTiter-Glo assay. Significance determined using 1-way ANOVA with Dunnett test. RLU = relative light units.

    Article Snippet: The MOC2( PD-L1 ) cell line was generated in our laboratory to overexpress PD-L1 by transducing MOC2 cells with a lentiviral vector carrying the murine CD274 gene tagged with a green fluorescent protein (GFP) reporter (MR 203953L2; OriGene Technologies).

    Techniques: Incubation, Expressing, In Vitro, Glo Assay

    (A) LoM were administered a single intramuscular dose of palivizumab 24 h prior to RSV A2-GFP exposure (15mg/kg or 30mg/kg) or 24 h post-RSV A2-GFP exposure (30mg/kg). Untreated RSV-GFP infected LoM served as a control. (B) GFP+ cells in human lung implants 4 days post-RSV exposure in untreated LoM (n=7 implants) and LoM administered palivizumab pre (15 mg/kg, n=6 implants and 30 mg/kg, n=3 implants) or post (n=4 implants) RSV exposure. (C) Ribavirin was administered to mice once daily (40 mg/kg, intraperitoneal) starting 24 h before or after RSV exposure. Untreated RSV-Luc infected LoM served as a control. (D) Bioluminescence signal (radiance [p sec–1 cm–2 sr–1] represented as total flux) in human lung implants just prior to RSV-exposure and 7 days post-RSV exposure in untreated LoM (white bars, n= 5 implants) and LoM administered ribavirin treatment initiated pre (orange bars, n=6 implants) or post (green bars, n= 6 implants) RSV exposure. The mean (horizontal line) and standard deviation (vertical line) are shown. Background luminescence measured pre-exposure is denoted by the dashed line. (E) Immunohistochemical staining for RSV antigen (brown) in human lung implants 7 days post RSV exposure in untreated LoM (left panel) and LoM administered ribavirin treatment-initiated pre (middle panel) or post (right panel) RSV exposure (scale bars, 100 um; n=3 implants analyzed). (B and D) Data are shown as mean ± SD. Results from treated groups were compared to untreated controls using a two-tailed Kruskal-Wallis test and P values were adjusted for multiple testing using the Benjamini, Krieger, Yekutieli false-discovery rate method.

    Journal: Frontiers in virology (Lausanne, Switzerland)

    Article Title: RSV infection of humanized lung-only mice induces pathological changes resembling severe bronchiolitis and bronchopneumonia

    doi: 10.3389/fviro.2024.1380030

    Figure Lengend Snippet: (A) LoM were administered a single intramuscular dose of palivizumab 24 h prior to RSV A2-GFP exposure (15mg/kg or 30mg/kg) or 24 h post-RSV A2-GFP exposure (30mg/kg). Untreated RSV-GFP infected LoM served as a control. (B) GFP+ cells in human lung implants 4 days post-RSV exposure in untreated LoM (n=7 implants) and LoM administered palivizumab pre (15 mg/kg, n=6 implants and 30 mg/kg, n=3 implants) or post (n=4 implants) RSV exposure. (C) Ribavirin was administered to mice once daily (40 mg/kg, intraperitoneal) starting 24 h before or after RSV exposure. Untreated RSV-Luc infected LoM served as a control. (D) Bioluminescence signal (radiance [p sec–1 cm–2 sr–1] represented as total flux) in human lung implants just prior to RSV-exposure and 7 days post-RSV exposure in untreated LoM (white bars, n= 5 implants) and LoM administered ribavirin treatment initiated pre (orange bars, n=6 implants) or post (green bars, n= 6 implants) RSV exposure. The mean (horizontal line) and standard deviation (vertical line) are shown. Background luminescence measured pre-exposure is denoted by the dashed line. (E) Immunohistochemical staining for RSV antigen (brown) in human lung implants 7 days post RSV exposure in untreated LoM (left panel) and LoM administered ribavirin treatment-initiated pre (middle panel) or post (right panel) RSV exposure (scale bars, 100 um; n=3 implants analyzed). (B and D) Data are shown as mean ± SD. Results from treated groups were compared to untreated controls using a two-tailed Kruskal-Wallis test and P values were adjusted for multiple testing using the Benjamini, Krieger, Yekutieli false-discovery rate method.

    Article Snippet: Viruses and in vivo analysis of infection Stocks of RSV strain A2 expressing green fluorescent protein (GFP) ( 21 ) or firefly luciferase (Luc) reporter genes were obtained from Viratree.

    Techniques: Infection, Control, Standard Deviation, Immunohistochemical staining, Staining, Two Tailed Test