Present address: Nutrition & Metabolism Center, Children’s Hospital Oakland Research Institute, Oakland CA 94609, USA.
Identification of age-specific Nrf2 binding to a novel antioxidant response element locus in the Gclc promoter: a compensatory means for the loss of glutathione synthetic capacity in the aging rat liver?
Article first published online: 1 FEB 2012
© 2011 The Authors. Aging Cell © 2011 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland
Volume 11, Issue 2, pages 297–304, April 2012
How to Cite
Shenvi, S. V., Smith, E. and Hagen, T. M. (2012), Identification of age-specific Nrf2 binding to a novel antioxidant response element locus in the Gclc promoter: a compensatory means for the loss of glutathione synthetic capacity in the aging rat liver?. Aging Cell, 11: 297–304. doi: 10.1111/j.1474-9726.2011.00788.x
- Issue published online: 15 MAR 2012
- Article first published online: 1 FEB 2012
- Accepted manuscript online: 28 DEC 2011 03:10PM EST
- Accepted for publication 14 December 2011
Data S1 Experimental procedures.
Table S1 Primers used for ChIP analysis of Gclc promoter elements.
Table S2 Sequence of Inserts in the pGL4 minimal promoter vector.
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