Cells were crosslinked with 1% formaldehyde and then lysed in SDS lysis buffer (50 mM Tris-HCl, pH 8.0, 1% SDS, 10 mM EDTA, and protease inhibitors). The ChIP procedure was performed as previously described [24]. Primer sequences are listed in Table 2.
Primer sets for ChIP-qPCR.
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