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Manufactured under cGMP standards and shipped domestically from Sarasota, FL, this compound is used in in-vitro studies on angiogenesis, epithelial barrier function, and extracellular matrix modulation

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The applicability of these technologies has been demonstrated by approvals of ADCs (e.g., trastuzumab emtansine in 2013, trastuzumab deruxtecan in 2019, and sacituzumab govitecan in 2020), the first BiTE (blinatumomab in 2014), and the first nanobody (caplacizumab in 2019)

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