Fig. 2From: A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1Characterization of SM9-1 iPSCs. a Morphology of the established iPSC line SM9-1 (left panel: feeder-free condition, right panel: on-feeder condition). Scale bar, 100 μm. b PCR analysis for the detection of remaining oriP/EBNA1-based reprogramming vectors. c Karyotype analysis of SM9-1 iPSCs. d Sanger sequencing of the targeted mutation site of HTRA1 gene (c.905G>A, p. R302Q, heterozygous) in SM9-1 T lymphocytes and SM9-1 iPSCsBack to article page