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• W2022047689 abstract "As the use of adenoviral vectors in gene therapy protocols increases, there is a corresponding need for rapid, accurate, and reproducible titer methods. Multiple methods currently exist for determining titers of recombinant adenoviral vector, including optical absorbence, electron microscopy, fluorescent focus assay, and the “gold standard” plaque assay. This paper introduces a novel flow cytometric method for direct titer determination that relies on the expression of the green fluorescent protein (GFP), a tracking marker incorporated into several adenoviral vectors. This approach was compared to the plaque assay using 10−4-to 10−6-fold dilutions of a cesium-chloride-purified, GFP expressing adenovirus (AdEasy+GFP+GAL). The two approaches yielded similar titers: 3.25±1.85×109 PFU/mL versus 3.46±0.76×109 green fluorescent units/(gfu/mL). The flow cytometric method is complete within 24 h in contrast to the 7×10 days required by the plaque assay. These results indicate that the GFU/mL is an alternative functional titer method for fluorescent-tagged adenoviral vectors." @default.
• W2022047689 created "2016-06-24" @default.
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• W2022047689 date "2000-03-01" @default.
• W2022047689 modified "2023-10-05" @default.
• W2022047689 title "A flow cytometric protocol for titering recombinant adenoviral vectors containing the green fluorescent protein" @default.
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• W2022047689 doi "https://doi.org/10.1385/mb:14:3:197" @default.
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