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The ChIP-Chip hybridization used a Roche Nimblegen's Rat ChIP-chip 3×720K RefSeq Promoter Array. Purified DNA was checked on the gel and sent to Nimblegen for ChIP-chip hybridization (Nimblegen, Iceland). Testis samples were mixed with SL2 cells and homogenized to make single cell suspension. Enlast Reviews – Does This Product Really Work? Loss of SOX9 induced profound apoptosis of TNBC cells, with only a slight impairment of the G1 to S cell cycle progression, demonstrating that SOX9 is required for cancer survival. Transcription factors (TFs) are critical molecules that regulate gene expression, ultimately controlling biologic processes such as cell growth, survival, and metastasis. Using CHIP assays, we demonstrated that SOX9 directly binds the promoters of genes involved in EMT (vim, cldn1, ctnnb1, and zeb1) and that SOX9 knock-down suppresses the expression of these genes. Based on published CHIP-seq data, we demonstrated that SOX9 binds to the promoter of apoptosis-regulating genes (tnfrsf1b, fadd, tnfrsf10a, tnfrsf10b, and ripk1), and represses their expression. Wellness Digest participates in various affiliate marketing programs, which means we may get paid commissions on editorially chosen products purchased through our links to retailer sites. By contrast, the DNA segments in the 5′ promoter (−743/−676) and intron 4 (+1450/+1530), where a SOX9 interaction site was not detected by ChIP-on-chip, were not amplified when anti-SOX9-ChIP DNA was used as a template (Fig. 2B). We observed a strong amplification region in the Ctgf gene near the peak detected by ChIP-on-chip. To validate the SOX9 interaction site obtained from the ChIP-on-chip experiment, qPCR was performed using the anti-SOX9-ChIP DNA as a template. (A) ChIP-on-chip using aSOX9 antibody showed a specific hybridization peak near the transcription initiation site in the Ctgf gene. 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