EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit

ChIP Human - ASM

Experiment
ChIP Human - ASM
Product
EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit from Merck Millipore
Manufacturer
Merck Millipore

Protocol tips

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

ChIP analysis was carried using the Magna ChIPTM A/G chromatin immunoprecipitation kit following the manufacturer's instructions (Merck Millipore, Watford, UK). In brief, ASM cells were grown in culture and treated as described above. Following stimulation the cells were formalin-fixed. The cells were sonicated to shear DNA (5 × 15 s at 40% amplitude) to ∼200–1000 bp in length. Brd4 and c-Myc were immunoprecipitated using 1 μg of antibody (Santa Cruz Biotechnology, Santa Cruz, CA). After reverse cross-linking, the DNA was purified and quantitative PCR carried out using SybrGreen (Qiagen) and the following primers: pCXCL8 forward, 5′-GGGCCATCAGTTGCAAATC-3′; pCXCL8 reverse, 5′-TCCTTCCGGTGGTTTCTTC-3′; pIL6 forward, 5′-CAAGCCTGGGATTATGAAGAAGG-3′; and pIL6 reverse, 5′-AGCACTGGCAGCACAAGGCAAAC-3′. The amount of DNA recovered by ChIP was normalized to an input control. IgG isotype antibodies (provided by Millipore) were used as a negative control for the ChIP assay.

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Papers

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Manufacturer protocol

Download the product protocol from Merck Millipore for EZ-Magna ChIP™ A/G Chromatin Immunoprecipitation Kit below.

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