An additional clone from this iPS cell line (PENN147i-M9-7) is available from WiCell.

  • Cell Line Alias M9-9
  • Unit of Measure (UOM) vial
  • Cell Type Human iPS
  • Sex Male
  • Age at Collection 22 Years
  • Ethnicity Information Self-reported
  • Reprogramming Method Non-integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
  • Tissue Origin Blood
  • Genetic Alteration Mutation Information Zygosity compound heterozygous, Allele1 p.W483X (old aa No: p. W462X), Allele 2 p.G549D (old aa No: p.G528D) http://www.ncbi.nlm.nih.gov/gene/3718
  • Diagnosis Information Diagnosis of Homozygous Familial Hypercholesterolemia was physician reported. Age at diagnosis was 3 Years of age. Additional diagnosis of aortic valve stenosis was also reported.
  • Disease Homozygous Familial Hypercholesterolemia
  • Ethnicity Caucasian
  • Genetic Alteration Mutation LDLR(del exon4-6)het
  • Provider University of Pennsylvania - Dr. Daniel Rader
  • Collections
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Lot Number Culture Platform Lot Description Banked By Passage Number Protocol Product Info URL
DB36419 Stem Cell Culture Medium (KOSR/MEF) Provider 18 WiCell Feeder Based (MEF) Pluripotent Stem Cell Protocol PDF

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