Standard Culture of Human Embryonic Stem Cells

Jeremy M. Crook, Rachel Horne, Alan Colman

Research output: Chapter in Book or Conference Publication/ProceedingChapterpeer-review

2 Citations (Scopus)

Abstract

Traditional methods of human embryonic (ES) cell maintenance have evolved over the last number of years, culminating in a myriad of published protocols with variable proficiencies with different cell lines. Accordingly, there is a need for standardized and reliable protocols that can be used with a broad range of human ES cell lines. The chapter is divided into two sections: 'routine' and 'extended' protocol sections. In the routine section, protocols such as culturing, freezing and thawing human ES cells on mouse feeders, testing for contamination, and disaggregation in standard (serum replacement containing) human ES cell medium are included. This, in addition to work described in the preceeding chapter, should be suffieient to get a novice laboratory proficient in culturing most of the human ES cell lines available. The extended protocol section includes vitrification, culture on human feeders, feeder-free culture, trypinization, culture on matrigel, and controlled rate freezing, and while not as pervasively used as routine protocols are still useful to the veteran human embryonic stem cell laboratory.

Original languageEnglish
Title of host publicationHuman Embryonic Stem Cells
Subtitle of host publicationThe Practical Handbook
PublisherJohn Wiley & Sons, Ltd
Pages53-79
Number of pages27
ISBN (Print)9780470033562
DOIs
Publication statusPublished - 15 Jun 2007
Externally publishedYes

Keywords

  • Cryopreservation
  • Cryostatsis
  • Culture
  • Disaggregation
  • Feeder
  • Feeder-free
  • Freezing
  • Human embryonic stem cell
  • Microdissection
  • Subculture
  • Thawing
  • Vitrification

Fingerprint

Dive into the research topics of 'Standard Culture of Human Embryonic Stem Cells'. Together they form a unique fingerprint.

Cite this