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. 2018 Mar 8;19(3):770. doi: 10.3390/ijms19030770

Table 1.

Methods for iPSC generation and quality control in BD studies.

Ref. Source Factors Methods Auth Karyo Pluripotency
[63] FB OKSM RV ≥5 nd nd ICC, EB and TriL
[64] FB miR/NAM LV na na na ICC
[65] FB OKSM RV ≥3 SNP G-Band ICC, PluriTest, EB and ScoC, Tera
[66] FB OKSM SV 2 nd G-Band ICC, TriL
[67] FB miR/NAM LV na na na ICC
[68] FB OKSM SV 3 nd G-Band ICC, EB and TriL
[69] LCL OKSM, LIN28 Epi ≥3 STRP nd ICC
[70] FB, LB OKSM Epi, LV, RV 1–3 SNP nd ICC, PluriTest, EB, Tera
[71] AP OKSM Epi 1 nd nd ICC, EB and TriL

AP, adipocytes; Auth, authentication; EB, undirected embryoid body formation; Epi, episomal plasmid; FB, fibroblast; G-Band, chromosomal G-banding; ICC, immunocytochemistry; Karyo, karyotype; LB, lymphoblast from blood; LCL, lymphoblastoid cell line; LV, lentiviral transduction; miR/NAM, miR9/9*-124, NEUROD2, ASCL1, and MYT1L; OKSM, OCT4, KLF4, SOX2, MYC; N°, numbers of independent clones per donor; na, not applicable; nd, not determined; PluriTest, a bioinformatic approach to asses pluripotency [72]; Tera, teratoma formation; TriL, analysis of trilineage formation by ICC and/or qRT-PCR; Ref, reference; RV, retroviral transduction; ScoC, lineage score card [73]; SNP, whole genome single nucleotide profiling; SV, Sendai virus transduction; STRP, short tandem repeat profile.