Microglia are implicated in aging, neurodegeneration, and Alzheimer’s disease (AD). Traditional, low-plex, imaging methods fall short of capturing in situ cellular states and interactions in the human
Figure S1. FACS and MACS sorted HPCs differentiate into equivalent microglia as unsorted HPCs. Hierarchical clustering of all iPSmicroglia 2.0 samples show that MACS (fuchsia) and FACS (purple) sortin
Microglia-like cells and neural cells were generated from several hES and hIPS lines. As subset was characterized by RNA seq and compared to expression profiles of published primary and induced sample
