| Literature DB >> 28287577 |
Mandi J Corenblum1, Lalitha Madhavan2.
Abstract
There is great interest in utilizing human induced pluripotent stem cells (hiPSCs) for disease modeling and cell therapeutics due to their patient specificity and characteristic stemness. However, the pluripotency of iPSCs, which is essential to their functionality, must be confirmed before these cells can be used in such applications. While a rigorous characterization of iPSCs, through different cellular and functional assays is necessary to establish their pluripotency, routine assessment of pluripotency maintenance can be achieved more simply and effectively through immunocytochemical techniques. Here, we present a systematic protocol for culturing hiPSCs, in a scaled-down manner, to particularly facilitate the verification of their pluripotent state using immunocytochemistry. More specifically, this methodology encompasses an efficient and cost-effective means of growing iPSCs in serum-free conditions and plating them on small chamber slides or glass coverslips ideal for immunocytochemistry.Entities:
Mesh:
Year: 2017 PMID: 28287577 PMCID: PMC5408898 DOI: 10.3791/55260
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355