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. Author manuscript; available in PMC: 2014 Jul 14.
Published in final edited form as: Stem Cells. 2014 Jan;32(1):269–278. doi: 10.1002/stem.1545

Table 1. PV-specific and control iPSC lines used in this study.

iPSC clone Donor JAK2 WT
allele
JAK2 V617F
allele
BC1 Healthy donor 2 0
TNC1 Sickle cell anemia 2 0
iPV183 PV patient #1 1 1
PVB1.11 PV patient #2 2 0
PVB1.15 2 0
PVB1.4 0 2
PVB1.18 0 2

A panel of iPSCs derived from healthy donors and PV patients were used for this study. In addition to a healthy donor- and a sickle cell anemia patient-derived iPSCs, two clones generated from a PV patient’s blood cells also contained only wild-type JAK2 alleles (WT/WT). iPSC clones with homozygous JAK2 V617F mutation (V617F/V617F) were derived from the same PV patient. iPSCs with heterozygous JAK2 (WT/V617F) were derived from a separate PV patient in a previous study [33].

Abbreviations: iPSC, induced pluripotent stem cell; PV, polycythemia vera.