Hi, could you give me an advice about chromatin immunoprecipitation in bacteria? Is it possible to use DNase for removal nonbinding part of DNA? I mean this: protein will be bind on part of digested DNA, you will use DNase for removal part of DNA, which doesn´t bind my protein. Theoretically, it will remain only concrete part of DNA that bind my protein, because the protein protect phosphodiester bound. What do you think?