Present address: Alec N. Sexton, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3200, USA.
Age-associated increase in heterochromatic marks in murine and primate tissues
Version of Record online: 30 DEC 2010
© 2010 The Authors. Aging Cell © 2010 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland
Volume 10, Issue 2, pages 292–304, April 2011
How to Cite
Kreiling, J. A., Tamamori-Adachi, M., Sexton, A. N., Jeyapalan, J. C., Munoz-Najar, U., Peterson, A. L., Manivannan, J., Rogers, E. S., Pchelintsev, N. A., Adams, P. D. and Sedivy, J. M. (2011), Age-associated increase in heterochromatic marks in murine and primate tissues. Aging Cell, 10: 292–304. doi: 10.1111/j.1474-9726.2010.00666.x
- Issue online: 13 MAR 2011
- Version of Record online: 30 DEC 2010
- Accepted manuscript online: 22 DEC 2010 12:01PM EST
- Accepted for publication 19 November 2010
Fig. S1 Titration of antibody dilutions to determine saturating concentrations for quantitative signal detection.
Fig. S2 Flow cytometric analysis of the DNA content of early passage growing, quiescent, and late passage senescent HDF cells.
Fig. S3 Assessment of mH2A1 mRNA expression in HDF and murine tissues.
Fig. S4 Quantitative single cell measurements of mH2A protein levels in baboon skin.
Fig. S5 Quantitative single cell measurements of mH2A protein levels in MEF and tissues of mH2A1 knockout mice.
Table S1 Saturating concentrations of antibodies used in this study.
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