Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
-Ensure that all buffers are in clear solution. Shake or vortex if these buffers precipitate.
|
-When processing spin columns, always cap spin columns before placing them in the microcentrifuge.
-The conditions of crosslinked DNA shearing can be optimized based on cells and sonicator
equipment. If desired, remove 5 µl of sonicated cell lysate for agarose gel analysis. The length of sheared DNA should be between 200-1000 bp. |
|
Upstream tips |
-Ensure that all buffers are in clear solution. Shake or vortex if these buffers precipitate.
|
Protocol tips |
-When processing spin columns, always cap spin columns before placing them in the microcentrifuge.
-The conditions of crosslinked DNA shearing can be optimized based on cells and sonicator
equipment. If desired, remove 5 µl of sonicated cell lysate for agarose gel analysis. The length of sheared DNA should be between 200-1000 bp. |
Publication protocol
The ChIP assays were performed using an EpiQuikTM chromatin immunoprecipitation kit from Epigentek Group Inc. (Brooklyn, NY) and according to the published methods.
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Manufacturer protocol
Download the product protocol from Epigentek for EpiQuik Chromatin Immunoprecipitation (ChIP) Kit below.
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