Unit

UNIT 1B.9 Quantification of Pluripotency Transcription Factor Levels in Embryonic Stem Cells by Flow Cytometry

  1. Nicola Festuccia,
  2. Ian Chambers

Published Online: 1 DEC 2011

DOI: 10.1002/9780470151808.sc01b09s19

Current Protocols in Stem Cell Biology

Current Protocols in Stem Cell Biology

How to Cite

Festuccia, N. and Chambers, I. 2011. Quantification of Pluripotency Transcription Factor Levels in Embryonic Stem Cells by Flow Cytometry. Current Protocols in Stem Cell Biology. 19:B:1B.9:1B.9.1–1B.9.13.

Author Information

  1. Institute for Stem Cell Research, School of Biological Sciences, University of Edinburgh, Edinburgh, Scotland, United Kingdom

Publication History

  1. Published Online: 1 DEC 2011
  2. Published Print: DEC 2011

Abstract

Embryonic stem (ES) cell lines are derived from the inner cell mass of the pre-implantation blastocyst and are characterized by the ability to undergo indefinite self-renewal while retaining the potential to differentiate into each of the three primary germ layers. The ability of individual ES cells to self-renew or appropriately respond to differentiation signals is influenced by the intracellular level of a number of crucial transcription factors. It is therefore important to be able to reliably quantify the levels of these proteins in single cells. Here we present an intracellular staining technique for flow cytometry suitable for monitoring transcription factor expression in ES cells. We illustrate the application of this technique to the detection of Oct4 and Nanog proteins and the coupling of this approach with fluorescent reporters of gene activity. Curr. Protoc. Stem Cell Biol. 19:1B.9.1-1B.9.13. © 2011 by John Wiley & Sons, Inc.

Keywords:

  • ES cells;
  • FACS;
  • quantitation;
  • intracellular staining;
  • Nanog Oct4