it’s a good question to ask I agree. But I would imagine that even if IPSC MSCs also used 3D scaffolding technology, it would still put the batch quantities and quality vastly ahead of bone marrow derived technologies also using 3D scaffolding due to the same issue of batch to batch variability and senescence?
perhaps we can ask Killian for an answer to this.As Killian knows both techs more than most
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it’s a good question to ask I agree. But I would imagine that...
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