hiPSC lines were manually picked, passaged on human embryonic stem cell-qualified Matrigel-coated plates (0.05 mg/mL; BD Biosciences, Franklin Lakes, NJ, USA), and cultured in mTeSR1 medium (Stem Cell Technologies, Vancouver, BC, Canada) with Y-27632 ROCK inhibitor (Stem Cell Technologies, Vancouver, Canada), and under a feeder-free condition, preserving the stability for over 30 and more passages. The stemness characteristics and karyotype were also verified (data not shown).
Reprogramming Fibroblasts to hiPSCs
hiPSC lines were manually picked, passaged on human embryonic stem cell-qualified Matrigel-coated plates (0.05 mg/mL; BD Biosciences, Franklin Lakes, NJ, USA), and cultured in mTeSR1 medium (Stem Cell Technologies, Vancouver, BC, Canada) with Y-27632 ROCK inhibitor (Stem Cell Technologies, Vancouver, Canada), and under a feeder-free condition, preserving the stability for over 30 and more passages. The stemness characteristics and karyotype were also verified (data not shown).
Corresponding Organization : University of Rome Tor Vergata
Other organizations : Istituto di Farmacologia Traslazionale, University of Toronto, Nevada System of Higher Education, Istituto Neurologico Mediterraneo, University of Nevada, Reno
Variable analysis
- Fibroblast reprogramming into human-induced pluripotent stem cells (hiPSCs)
- Stemness characteristics
- Karyotype
- Healthy donor subject (wild type, WT, 46 XX, age 46)
- Dermal biopsy
- Informed written consent
- Project approval by The Committees on Health Research Ethics of Tor Vergata Hospital (2932/2017)
- Feeder-free culture condition
- Matrigel-coated plates (0.05 mg/mL; BD Biosciences, Franklin Lakes, NJ, USA)
- MTeSR1 medium (Stem Cell Technologies, Vancouver, BC, Canada)
- Y-27632 ROCK inhibitor (Stem Cell Technologies, Vancouver, Canada)
- Passaging and maintaining hiPSC lines for over 30 and more passages
- Not explicitly mentioned
- Not explicitly mentioned
Annotations
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