fluorescence imaging system Search Results


clinx chemiluminescence system  (Clinx Science)
96
Clinx Science clinx chemiluminescence system
Clinx Chemiluminescence System, supplied by Clinx Science, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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clinx chemiluminescence system - by Bioz Stars, 2026-06
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zoe fluorescent cell imager  (Bio-Rad)
96
Bio-Rad zoe fluorescent cell imager
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Zoe Fluorescent Cell Imager, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
zoe fluorescent cell imager - by Bioz Stars, 2026-06
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neutrophil elastase 680 fast imaging agent  (Revvity)
91
Revvity neutrophil elastase 680 fast imaging agent
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Neutrophil Elastase 680 Fast Imaging Agent, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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neutrophil elastase 680 fast imaging agent - by Bioz Stars, 2026-06
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mmpsense 645 fast  (Revvity)
91
Revvity mmpsense 645 fast
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Mmpsense 645 Fast, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mmpsense 645 fast - by Bioz Stars, 2026-06
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fluorescent western blotting  (Rockland Immunochemicals)
93
Rockland Immunochemicals fluorescent western blotting
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Fluorescent Western Blotting, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescent western blotting - by Bioz Stars, 2026-06
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chemiluminescence imaging system  (Clinx Science)
96
Clinx Science chemiluminescence imaging system
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Chemiluminescence Imaging System, supplied by Clinx Science, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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chemiluminescence imaging system - by Bioz Stars, 2026-06
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hypoxisense 680  (Revvity)
91
Revvity hypoxisense 680
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Hypoxisense 680, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ivi sense osteo 680 fluorescent probe  (Revvity)
91
Revvity ivi sense osteo 680 fluorescent probe
Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained <t>in</t> <t>ZOE‐Fluorescent</t> cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).
Ivi Sense Osteo 680 Fluorescent Probe, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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nev10149  (Revvity)
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Revvity nev10149
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Nev10149, supplied by Revvity, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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vivotrack 680 nir  (Revvity)
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750 fast  (Revvity)
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cat k 680 fast tm  (Revvity)
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Image Search Results


Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained in ZOE‐Fluorescent cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).

Journal: Journal of Cellular and Molecular Medicine

Article Title: Bioengineered AAV9 and Optimised Microdystrophin Vectors Augment Phenotypic Rescue in a Murine Model of Duchenne Muscular Dystrophy

doi: 10.1111/jcmm.71078

Figure Lengend Snippet: Validation of codon‐optimised microdystrophin transgene in vitro. Transduction of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys vectors in C2C12 cells (A), at an MOI: 1 × 10 5 and its quantification (B) are shown. Representative images were obtained in confocal microscope (AXR Nikon) with a 40X objective (Scale bar: 50 μm). Semi‐quantification was performed from images ( n ≥ 8 per group) obtained in ZOE‐Fluorescent cell imager. The data is represented as mean ± SD. Asterisk (*) represents statistical comparison of AAV9K51Q‐μDys and AAV9K51Q‐CoμDys treated conditions with respect to the cell control and Hash (#) refers to statistical comparison of AAV9K51Q‐CoμDys with respect to AAV9K51Q‐μDys. # p < 0.05, *** p < 0.001, **** p < 0.0001. For statistical comparison, a one‐way ANOVA was performed (GraphPad Prism 8.0.2 software).

Article Snippet: The images were obtained in the ZOE‐Fluorescent cell imager (Bio‐Rad, Hercules, CA, USA) and these images ( n ≥ 8/group) were further used for semi‐quantification analysis (ImageJ software).

Techniques: Biomarker Discovery, In Vitro, Transduction, Microscopy, Comparison, Control, Software

Dyes.

Journal: F1000Research

Article Title: A new analysis approach for single nephron GFR in intravital microscopy of mice

doi: 10.12688/f1000research.26888.3

Figure Lengend Snippet: Dyes.

Article Snippet: AngioSPARK 680 , NEV10149 , PerkinElmer , Vessel dye , 30 μl , 3 , 860 nm , 685–695 nm.

Techniques: