The EpiQuik™ Global Tri-Methyl Histone H4-K20 Quantification Kit (Colorimetric) is a complete set of essential components, which enables the experimenter to measure tri-methylation of histone H4-K20. The EpiQuik Global Tri-Methyl Histone H4-K20 Quantification Kit (Colorimetric) is suitable for using a variety of mammalian cells (human, mouse, etc.), including fresh and frozen tissues, and cultured adherent and suspension cells. The kit has the following advantages:
Background InformationEpigenetic activation or inactivation of genes plays a critical role in many important human diseases, especially in cancer. A major mechanism for epigenetic inactivation of the genes is methylation of CpG islands in genome DNA caused by DNA methyltransferases. Histone methyltransferases (HMTs) control or regulate DNA methylation through chromatin-dependent transcriptional repression or activation. HMTs transfer 1-3 methyl groups from S-adenosyl-Lmethionine to the lysine and arginine residues of histone proteins. PR-SET7, SET9, SUV4.20h, and ASH1are histone methyltransferases that catalyze methylation of histone H4 at lysine 20 (H4-K20) in mammalian cells. Tri-methylation of H4-K20 acts as a passive feature or structure determinant for chromatin degradation and release, as well as being an epigenetic marker of early apoptosis. Tri-methylation of H4-K20 is also considered as a common hallmark of human cancer. The global H4-K20 tri-methylation can be changed by inhibition or activation of HMTs. Therefore, quantitative detection of global tri-methyl histone H4-K20 would provide useful information for better understanding epigenetic regulation of tumorigenesis and apoptosis, as well as for developing HMT-targeted drugs. The EpiQuik™ Global Tri-Methyl Histone H4-K20 Quantification Kit (Colorimetric) provides a tool for measuring tri-methylation of histone H4-K20.
Principle & ProcedureThis kit is designed for measuring global histone H4-K20 tri-methylation. In an assay with this kit, the tri-methylated histone H4 at lysine 20 is captured to strip wells coated with an anti-trimethyl H4-K20 antibody. The captured tri-methylated histone H4-K20 can then be detected with a detection antibody, followed by a color development reagent. The ratio of tri-methylated H4-K20 is proportional to the intensity of absorbance. The absolute amount of tri-methylated H4-K20 can be quantitated by comparing to the standard control.
Starting MaterialsInput material should be purified histone extracts. In general, the input amount should be from 50 ng to 200 ng per well of histone extracts.