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Re: NY1972 post# 129

Monday, 06/06/2022 6:59:02 PM

Monday, June 06, 2022 6:59:02 PM

Post# of 263
They start with healthy donor fibroblasts, reprogram to create an iPSC pool and engineer using CRISPR (anti-MICA/B CAR, CD38 KO, IL-15RF and hnCD16 KI). After, comes single-cell sorting and screening of individual clones. The latter for extensive characterisation prior to master cell selection.

For that they look at clones with copy number and locus-target verification, maintain pluripotency, free of reprogramming vectors, demonstrate genomic stability, without off-target edits, ideal propensity to become NKs, as well as desired functional activity and specificity.
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