fluorescent protein gfp reporter (OriGene)
Structured Review

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
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
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 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 |
![(A) LoM were administered a single intramuscular dose of palivizumab 24 h prior to <t>RSV</t> <t>A2-GFP</t> 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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_9974/pmc11339974/pmc11339974__nihms-1996204-f0004.jpg)