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. 2016 Mar 25;44(13):6113–6126. doi: 10.1093/nar/gkw194

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© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 2. — ChIP-qPCR analysis of Abf1 and Fhl1 association to RP gene promoters. (A) Abf1 ChIP analysis was conducted using a strain carrying a TAP-tagged ABF1 allele. Fold-enrichment of the indicated RP gene promoters was calculated relative to HHT2 used as an internal standard. Positive (LTV1) and negative (FLR1) controls for Abf1 association were analyzed in the same experiment. (B) Fhl1 ChIP analysis was performed using a strain carrying a 13myc-tagged allele of FHL1. Positive (RPL28) and negative (FLR1) controls for Fhl1 association were analyzed in the same experiment. For both panels, data are the average of two independent replicates, with bars indicating the standard error.