S3-NTDi treated and untreated MB cells were protein-protein cross-linked with Disuccinimidyl glutarate (DSG), followed by protein-DNA cross-linked with formaldehyde, as described previously [26]. Cells were then lysed and sheared chromatin were immunoprecipitated with either STAT3 Ab or IgG, following instructions from Pierce Magnetic ChIP Kit (#26157). Quantitative genomic PCR was performed in QuantStudio 3 Real-Time PCR System, using human Bcl-2 promoter and CCND1 promoter primers (#12924, #12531) from Cell Signaling. Data were corrected for variations in input and expressed as fold change relative to IgG controls.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.