The EpiQuik™ Global Mono-Methyl Histone H3-K4 Quantification Kit (Colorimetric) is a convenient package of tools that allows the experimenter to specifically measure global Mono-methylation of histone H3-K4 colorimetrically, 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 play 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. SET1, SET7/9, Ash1, ALL-1, MLL, ALR, Trx, and SMYD3 are histone methyltransferases that catalyze methylation of histone H3 at lysine 4 (H3-K4) in mammalian cells. H3-K4 mono-methylation is associated with silenced euchromatin regions in the genome and may serve as a global epigenetic mark and function in gene repression. The global H3-K4 mono-methylation can also be changed by inhibition or activation of HMTs. Thus, quantitative detection of global mono-methyl histone H3-K4 would provide useful information for better understanding epigenetic regulation of gene activation/repression and for developing HMT-targeted drugs. The EpiQuik™ Global Mono-Methyl Histone H3-K4 Quantification Kit (Colorimetric) provides a tool for measuring global monomethylation of histone H3-K4.
Principle & ProcedureThis kit is designed for measuring global histone H3-K4 mono-methylation. In an assay with this kit, the mono-methylated histone H3 at lysine 4 is captured to the strip wells coated with an anti-monomethyl H3-K4 antibody. The captured mono-methylated histone H3-K4 can then be detected with a labeled detection antibody, followed by a color development reagent. The ratio of mono-methylated H3-K4 is proportional to the intensity of absorbance. The absolute amount of mono-methylated H3-K4 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.