Moody Jennifer
STEMCELL Technologies, Vancouver, BC, Canada.
Methods Mol Biol. 2013;946:507-21. doi: 10.1007/978-1-62703-128-8_31.
The continued success of pluripotent stem cell research is ultimately dependent on access to reliable and defined reagents for the consistent culture and cryopreservation of undifferentiated, pluripotent cells. The development of defined and feeder-independent culture media has provided a platform for greater reproducibility and standardization in this field. Here we provide detailed protocols for the use of mTeSR™1 and TeSR™2 with various cell culture matrices as well as defined cryopreservation protocols for human embryonic and human induced pluripotent stem cells.
多能干细胞研究的持续成功最终取决于能否获得可靠且明确的试剂,用于未分化多能细胞的一致培养和冷冻保存。明确的无饲养层培养基的开发为该领域实现更高的可重复性和标准化提供了一个平台。在这里,我们提供了使用mTeSR™1和TeSR™2与各种细胞培养基质的详细方案,以及人类胚胎干细胞和人类诱导多能干细胞的明确冷冻保存方案。