We have extended our Cell-Directed Integration (CDI) technology to mammalian cells!
We used Atomic Force Microscopy to demonstrate that integration into lipid-templated silica matrices enables a model mammalian cell (Hep3B) to remain viable for up to 1 week in the absence of any external buffer or growth medium.
Mammalian cells immobilized via CDI remain viable for ~1 week, even when stored/shipped without cold-chain.
Mammalian cells recovered from our lipid-templated silica matrices are able to divide normally.
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