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HDAd.Cre is a helper-dependent adenoviral (HDAd) vector designed to express Cre recombinase. HDAd vectors, also known as "gutless" adenoviruses, have all viral coding sequences removed, which significantly reduces immunogenicity and provides a large packaging capacity (up to 36 kb). In the context of the provided research, HDAd.Cre is utilized as a control or a validation tool for the in vivo engineering of hematopoietic stem and progenitor cells (HSPCs). It is used to demonstrate gene delivery and site-specific recombination in reporter mouse models (such as hCD46/Ai9), where Cre activity triggers the expression of fluorescent proteins like tdTomato. This vector is part of a broader platform developed by researchers at the University of Washington to enable the sustained production of engineered extracellular vesicles for the treatment of lysosomal storage disorders, including Pompe Disease.
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