The PCR products from branched intermediates obtained with primers P2a and P3a specific for nad1e and primers P2b and P3b specific for nad5c were purified from agarose gel and cloned into pGEM-T, subs
Figure S1. The pUC57-sgRNA expression vector. The sgRNA expression vector was constructed using the backbone of the pUC57 vector with a Kanamycin resistance gene. The annealed oligos were inserted bet
Improved understanding of mechanisms regulating myelodysplastic syndrome (MDS) hematopoietic stem/progenitor cell (HSPC) growth and self-renewal is critical for developing MDS therapy. We revealed a n