Our service includes reprogramming of patient, donor or primate samples to iPSCs using non-integrating Sendai virus, the banking and culturing of resulting stem cell lines and QC analysis, for exapmle of the karyotype, markers of the undifferentiated state and trilineage layer differentiation potential.

In addition, the facility established CRISPR/Cas9 mediated genome engineering to stably integrate (inducible) expression constructs, tag endogenous proteins, generate knockouts, fluorescence reporters or isogenic control lines. We offer homology directed repair (HDR), (adenine) base editing and prime editing for generation or correction of small mutations in wildtype and patient iPSC lines.