The EpiQuik Circulating Trimethyl Histone H3K4 ELISA Kit (Colorimetric) is a complete set of optimized buffers and reagents specifically is designed to quantitatively detect circulating histone H3K4me3 from plasma and serum. This 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 gene inactivation is methylation of CpG islands in genomic 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-L-methionine to the lysine and arginine residues of histone proteins. SETD1 and MLL are major histone methyltransferases that catalyze methylation of histone H3 at lysine 4 (H3-K4) in mammalian cells and KDM is the major histone demethylase that demethylates H3K4. Trimethyl H3K4 (H3K4me3) has been viewed as a signature mark of highly transcribed genes, which is placed exclusively in the 5’- region downstream of the promoter. The H3K4me3 can also be changed by inhibition or activation of HMTs. Circulating histone H3K4me3 in plasma or serum has been observed and demonstrated as the marker for many different diseases or pathological changes such as cancer progression. Therefore, detection of circulating H3K4me3 would provide useful information for a better understanding of epigenetic regulation of gene activation and silencing, histone modification-associated pathological processes, screening of disease-related biomarkers, as well as for developing histone modification-targeted drugs.
Principle & ProcedureThis kit is designed for measuring total H3K4me3 in plasma or serum. In an assay with this kit, the Histone H3 proteins trimethylated at K4 in the plasma/serum sample are captured on the strip wells coated with anti-H3K4me3 antibody. The captured H3K4me3 proteins can be then recognized with detection antibody followed by a color development reagent. The ratio of H3K4me3 is proportional to the intensity of absorbance. The absolute amount of H3K4me3 can be quantitated by comparing to the standard control.
Starting MaterialsInput materials should be plasma or serum. The amount of plasma or serum for each assay can be 10 to 40 µl with an optimal amount of 30 µl.