Figure 6
Figure 6. Chromatin remodeling (CHIP assay). HUVECs and HASMCs were treated with 50 μM DL-Hcy and 1 mM AZC in control medium for 48 hours, or 300 nM TSA and 5 mM NaBr for 24 hours. Nuclear extracts were immunoprecipitated with antibody against MeCP2 (A,B), and AcH3 or AcH4 (C). PCR was performed using primers specific for cyclin A promoter from position −267 to 37. Input DNA was amplified to evaluate the total amount of DNA applied to the immunoprecipitation.

Chromatin remodeling (CHIP assay). HUVECs and HASMCs were treated with 50 μM DL-Hcy and 1 mM AZC in control medium for 48 hours, or 300 nM TSA and 5 mM NaBr for 24 hours. Nuclear extracts were immunoprecipitated with antibody against MeCP2 (A,B), and AcH3 or AcH4 (C). PCR was performed using primers specific for cyclin A promoter from position −267 to 37. Input DNA was amplified to evaluate the total amount of DNA applied to the immunoprecipitation.

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