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- W4386475146 abstract "Lentiviral (LV) vector-based gene therapy is gaining popularity for treating a wide range of diseases. Various LV vectors are being developed for transducing cells in cellular gene therapy at St. Jude. Some LV vectors are produced using stable 293T packaging cell lines that includes gag-pol-rev-tat and virus-glycoprotein. Transactivating factor (Tat) is a regulatory protein that drastically increases the efficiency of lentiviral transcription. Residual analysis of Tat is a critical contribute for gene vector quality and safety. In this article, we developed a highly sensitive LC-MS/MS method for analysis of residual Tat in Lentivirus as an alternative to ELISA. Residual Tat in LV can be accurately quantified with high specificity and a LOD of 0.3 ng/mL." @default.
- W4386475146 created "2023-09-07" @default.
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- W4386475146 date "2023-09-06" @default.
- W4386475146 modified "2023-09-27" @default.
- W4386475146 title "Development and validation of an LC-MS/MS method for sensitive analysis of residual protein Tat Bh 1-101 in Lentiviral Vectors for Gene Therapy" @default.
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- W4386475146 doi "https://doi.org/10.1089/hum.2023.030" @default.
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