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Photobleaching Assays (FRAP & FLIP) to Measure Chromatin Protein Dynamics in Living Embryonic Stem Cells
Journal JoVE
Biologie
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Journal JoVE Biologie
Photobleaching Assays (FRAP & FLIP) to Measure Chromatin Protein Dynamics in Living Embryonic Stem Cells
DOI:

09:18 min

June 29, 2011

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Chapitres

  • 00:05Titre
  • 01:04Plating the Stem Cells
  • 02:02Transfecting the Stem Cells
  • 03:24Performing FRAP or FLIP
  • 06:10FRAP and FLIP Data Analysis
  • 07:26FRAP and FLIP Results
  • 08:52Conclusion

Summary

Traduction automatique

We describe photobleaching methods including Fluorescence Recovery After Photobleaching (FRAP) and Fluorescence Loss In Photobleaching (FLIP) to monitor chromatin protein dynamics in embryonic stem (ES) cells. Chromatin protein dynamics, which is considered to be one of the means to study chromatin plasticity, is enhanced in pluripotent cells.

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