Hi,
I am trying doing ChIPSeq for mouse heart homogenates (100mg). I changed the protocol conditions for different times, but I always have the same problem, that I see two peaks in the Agilent Bioanalyzer, the first required peak with ca.200bp and a big peak at >2kb.
I looked for different Cycle conditions, but I guess that I get mistakes in my sample preparation. How can I homogenize and handle the heart tissue in the right way?
Thanks!
I am trying doing ChIPSeq for mouse heart homogenates (100mg). I changed the protocol conditions for different times, but I always have the same problem, that I see two peaks in the Agilent Bioanalyzer, the first required peak with ca.200bp and a big peak at >2kb.
I looked for different Cycle conditions, but I guess that I get mistakes in my sample preparation. How can I homogenize and handle the heart tissue in the right way?
Thanks!