Key Spec Table
|5 vials||5-6x106 ea||Cult|
|Application||The PMEF feeders are treated with Mitomycin-C. These fibroblasts can be directly plated onto gelatin coated (See ES-006-B) culture vessels.|
|Cell Line Type||
|Safety Information according to GHS|
|Storage and Shipping Information|
|Storage Conditions||After receipt, vials should be stored at -80°C. If storing for longer than 6 months, store in the vapor phase of liquid nitrogen (make sure the cap is tight) for up to 2 years.|
|Reference overview||Pub Med ID|
|Transcriptional signature and memory retention of human-induced pluripotent stem cells. |
Marchetto, Maria C N, et al.
PLoS ONE, 4: e7076 (2009) 2009
Genetic reprogramming of somatic cells to a pluripotent state (induced pluripotent stem cells or iPSCs) by over-expression of specific genes has been accomplished using mouse and human cells. However, it is still unclear how similar human iPSCs are to human Embryonic Stem Cells (hESCs). Here, we describe the transcriptional profile of human iPSCs generated without viral vectors or genomic insertions, revealing that these cells are in general similar to hESCs but with significant differences. For the generation of human iPSCs without viral vectors or genomic insertions, pluripotent factors Oct4 and Nanog were cloned in episomal vectors and transfected into human fetal neural progenitor cells. The transient expression of these two factors, or from Oct4 alone, resulted in efficient generation of human iPSCs. The reprogramming strategy described here revealed a potential transcriptional signature for human iPSCs yet retaining the gene expression of donor cells in human reprogrammed cells free of viral and transgene interference. Moreover, the episomal reprogramming strategy represents a safe way to generate human iPSCs for clinical purposes and basic research.
|Establishment of rat embryonic stem cells and making of chimera rats. |
Ueda S. et al.
PLoS One 3(7) e2800 2008
The rat is a reference animal model for physiological studies and for the analysis of multigenic human diseases such as hypertension, diabetes, neurological disorders, and cancer. The rats have long been used in extensive chemical carcinogenesis studies. Thus, the rat embryonic stem (rES) cell is an important resource for the study of disease models. Attempts to derive ES cells from various mammals, including the rat, have not succeeded. Here we have established two independent rES cells from Wister rat blastocysts that have undifferentiated characters such as Nanog and Oct3/4 genes expression and they have stage-specific embryonic antigen (SSEA) -1, -3, -4, and TRA-1-81 expression. The cells were successfully cultured in an undifferentiated state and can be possible over 18 passages with maintaining more than 40% of normal karyotype. Their pluripotent potential was confirmed by the differentiation into derivatives of the endoderm, mesoderm, and ectoderm. Most importantly, the rES cells are capable of producing chimera rats. Therefore, we established pluripotent rES cell lines that are widely used to produce genetically modified experimental rats for study of human diseases.
|Murine Embryonic Stem Cell Culture Procedures & Protocols|
Technical Info and Required Licenses
|A Comparative Analysis of Human Embryonic Stem Cells Cultured in a Variety of Media Conditions|
|Single transfection of a synthetic polycistronic self-replicative RNA yields high numbers of transgene-free human iPSCs|