Supplemental text; Tables S1 (DNA sequences for EMSA experiments), S2 (Sequences to generate dsRNA), and S3 (Sequences for ChIP-qPCR targets); and Fig. S1 (GAF and CLAMP binding to the Fab-7 boundary in vivo), S2 (CLAMP in LBC binding to the Fab-7 GAGA5+6 sequence), S3 [CLAMP, GAF, and Mod(mdg4) cofractionation with LBC], S4 (Competition experiments with roX1 and roX2 DNAs), S5 (Cross competition of CES 5C2, CES 5C2 mut 1+2+3, and interacting CES), S6 (Supershift experiments), and S7 (LBC shift of CES CG14446 by Superose 6 column fractions)
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