Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/131596
DC FieldValue
dc.titlePropagation of human embryonic stem cells on human feeder cells.
dc.contributor.authorRichards, M.
dc.contributor.authorBongso, A.
dc.date.accessioned2016-11-29T01:20:31Z
dc.date.available2016-11-29T01:20:31Z
dc.date.issued2006
dc.identifier.citationRichards, M., Bongso, A. (2006). Propagation of human embryonic stem cells on human feeder cells.. Methods in molecular biology (Clifton, N.J.) 331 : 23-41. ScholarBank@NUS Repository.
dc.identifier.issn10643745
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/131596
dc.description.abstractHuman embryonic stem (hES) cell lines are usually derived and propagated on inactivated murine embryonic fibroblast (MEF) feeders. The use of MEFs and culture ingredients of animal origin for hES cell support increases the risk of cross-contamination of the hES cells with infectious animal agents from the MEFs and animal-based culture medium. This thus makes such hES cells lines undesirable for clinical application. This chapter describes several protocols used in the propagation of hES cells on human fibroblast feeder cells. Two culture methods, the bulk enzymatic culture protocol and the microdissection "cut and paste" protocol are described. Only certain human fetal and adult fibroblast feeders support hES cell growth. Methods for the characterization of pluripotent undifferentiated hES cells grown on human feeders including cell surface marker staining and real-time polymerase chain reaction are also described.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.description.sourcetitleMethods in molecular biology (Clifton, N.J.)
dc.description.volume331
dc.description.page23-41
dc.identifier.isiutNOT_IN_WOS
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.