, Triton X-100, 150 mM NaCl, 20 mM Tris-HCl, pH 8.1, 0.1% SDS, and 2 mM EDTA), 600 µL of TSE2 buffer (1% Triton X-100, 500 mM NaCl, 20 mM Tris-HCl, pH 8.1, 0.1% SDS, and 2 mM EDTA), and 600 µL of TSE3 buffer (1% NP40, 1% sodium deoxycholate, 250 mM LiCl, and 10 mM Tris-HCl, pH 8.1). Following two washes in TE buffer (10 mM Tris-HCl and 1 mM EDTA), samples were eluted with 200 µL of fresh elution buffer (1% SDS and
, DNA was purified using a High Pure PCR Template Preparation Kit (Roche) and analyzed by Q-PCR. Antibodies used: rabbit polyclonal anti-Myc (Cell Signaling 9402), rabbit polyclonal IgG control isotype (Cell Signaling 39005), or mouse monoclonal anti-GAL4 (Santa Cruz sc-510). The following region was amplified
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