Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
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-Just because an antibody works well in a Western blot does not always indicate it will perform well in chromatin immunoprecipitation.
Unlike a Western blot that detects proteins that have been denatured, a ChIP antibody must recognize the target protein in its native state. Use ChIP-validated antibody.
-Use 2-10 μg of your ChIP antibody depending on the abundance of your protein target. |
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Protocol tips |
-Just because an antibody works well in a Western blot does not always indicate it will perform well in chromatin immunoprecipitation.
Unlike a Western blot that detects proteins that have been denatured, a ChIP antibody must recognize the target protein in its native state. Use ChIP-validated antibody.
-Use 2-10 μg of your ChIP antibody depending on the abundance of your protein target. |
Publication protocol
Chromatin immunoprecipitation (ChIP) assays were performed using the ChIP Assay Kit (Millipore, Billerica, USA). Rat liver tissues were homogenised and fixed with 1% formaldehyde. DNA was sheared to 200–1000 bp fragments using sonication. Chromatin was incubated and precipitated with antibodies against FXR, histone deacetylase 3 (HDAC3; Epitomics), or IgG (Boster, Wuhan, China). Primers used to amplify the binding site of FXR on the promoter region of MRP2 gene for qPCR were designed as follows: sense- 5’-agagtgagttccaggacagt-3’; antisense- 5’-ccctgtagtgtgaccaaata-3’.
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Manufacturer protocol
Download the product protocol from Merck Millipore for Chromatin Immunoprecipitation (ChIP) Assay Kit below.
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