The EpiQuik™ Global Di-Methyl Histone H3-K27 Quantification Kit (Fluorometric) is a convenient package of tools that allows the experimenter to specifically measure global di-methylation of histone H3-K27 fluorometrically using a variety of mammalian cells (human, mouse, etc.) including fresh and frozen tissues, 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 transcription repression or activation. HMTs transfer 1-3 methyl groups from S-adenosyl-Lmethionine to the lysine and arginine residues of histone proteins. G9a and polycomb group enzymes such as EZH2 are histone methyltransferases that catalyze methylation of histone H3 at lysine 27 (H3-K27) in mammalian cells. Histone H3-K27 di-methylation, a modification enriched at pericentromeric heterochromatin, is observed to be broadly distributed throughout all euchromatic sites and participates in silencing gene expression. Increased global H3-K27 di– and tri-methylation is found to be involved in some pathological processes such as cancer progression. The global H3-K27 di-methylation can be also changed by inhibition or activation of HMTs. Thus quantitative detection of global di-methyl histone H3-K27 would provide useful information for better understanding epigenetic regulation of gene activation/repression and for developing HMTtargeted drugs. The EpiQuik™ Global Di-Methyl Histone H3-K27 Quantification Kit (Fluorometric) provides a tool for measuring global di-methylation of histone H3-K27.
Principle & ProcedureThis kit is designed for measuring global histone H3-K27 di-methylation. In an assay with this kit, the di-methylated histone H3 at lysine 27 is captured to the strip wells coated with an anti-dimethyl H3-K27 antibody. The captured di-methylated histone H3-K27 can then be detected with a labeled detection antibody, followed by a fluorescent development reagent. The ratio of di-methylated H3-K27 is proportional to the intensity of fluorescence. The absolute amount of di-methylated H3-K27 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.