Epigentek Home
EpiGentek Guarantee

EpiQuik Histone H3 Modification Multiplex Assay Kit (Colorimetric)


For ELISA-like quantitation of 21 different histone H3 modification patterns on the same plate

Citations (12) | (1) | Write a Review
Suggested Workflow
Histone Protein Extraction
Histone Modification Quantification
Histone extracts were prepared from MCF-7 and MDA-231 cells using the EpiQuik™ Total Histone Extraction Kit (Cat. No. OP-0006) and multiple histone H3 modifications were screened and measured using the EpiQuik™ Histone H3 Modification Multiplex Assay Kit (Colorimetric). 100 ng of total histone proteins were used.
Schematic procedure for the EpiQuik™ Histone H3 Modification Multiplex Assay Kit (Colorimetric).
Working principle of the EpiQuik™ Histone H3 Modification Multiplex Assay Kit (Colorimetric).
Input Type: Histone Extracts
Research Area: Histone Methylation
Target Application: Amount Quantitation
Vessel Format: 96-Well Plate
100% Guarantee: 6 months
Catalog No.SizePriceQty
P-3100-9696 assays $719.00 
Order now & get it by Thursday, November 14th  
Product Overview

The EpiQuik™ Histone H3 Modification Multiplex Assay Kit (Colorimetric) is a complete set of optimized reagents to detect and quantify up to twenty-one (21) modified histone H3 patterns simultaneously in a simple, ELISA-like format with use of a standard microplate reader. The kit has the following advantages and features:

  • Simultaneously screen and measure 21 different histone H3 modifications, which includes all of the most important and the most well-characterized patterns.
  • Quick and efficient procedure, which can be finished within 2 hours and 30 minutes.
  • Innovative colorimetric assay without the need for radioactivity, electrophoresis, chromatography, or expensive equipment.
  • High sensitivity with a detection threshold as low as 0.5 ng/well for each modification pattern and a detection range from 20 ng to 500 ng/well of histone extracts.
  • An assay control is conveniently included for quantification of each histone H3 modification.
  • Total histone H3 sets are included, which can be used for normalizing total histone H3 levels for relative comparison of histone H3 content between different samples or different treatment conditions.
  • Strip microplate format makes the assay flexible: manual or high throughput, which enables analysis of a single modification or total 21 modification patterns within the same samples.
  • Two extra 8-well strips are included in the kit which can be used, if necessary, for sample amount pre-optimization to determine the input amount (ex: 50, 100, 200 ng/well) needed to fall within the detection limits of the assay. Extra strips may also be used as assay controls and total histone level controls if selective detection of some histone H3 modifications from the total 21 modification pattern is desired.
  • Simple, reliable, and consistent assay conditions.

Background Information
Histone modifications have been defined as epigenetic modifiers. Post-translational modifications (PTMs) of histones include the acetylation of specific lysine residues by histone acetyltransferases (HATs), deacetylation by histone deacetylase (HDACs), the methylation of lysine and arginine residues by histone methytransferases (HMTs), the demethylation of lysine residues by histone demethylases (HDMTs), and the phosphorylation of specific serine groups by histone kinases (HKs). Additional histone modifications include the attachment of ubiquitin (Ub), small ubiquitin-like modifiers (SUMOs), and poly ADP-ribose (PAR) units. Next to DNA methylation, histone acetylation and histone methylation are the most well characterized epigenetic marks. Generally, tri-methylation at H3-K4, H3-K36, or H3-K79 results in an open chromatin configuration and is therefore characteristic of euchromatin. Euchromatin is also characterized by a high level of histone acetylation, which is mediated by histone acetyltransferases. Lysine residues can be mono-, di-, or tri-methylated, each of which can differentially regulate chromatin structure and transcription. Along with other histone modifications such as phosphorylation, this enormous variation leads to a multiplicity of possible combinations of different modifications. This may constitute a “histone code”, which can be read and interpreted by different cellular factors.

Principle & Procedure
In an assay with this kit, each histone H3 modified at specific sites will be captured by an antibody that is coated on the strip wells and specifically targets the appropriate histone modification pattern. The captured histone modified at specific sites will be detected with a detection antibody, followed by a color development reagent. The ratio of modified histone is proportional to the intensity of absorbance measured by a microplate reader at a wavelength of 450 nm.

Starting Materials
Input materials can be histone extracts or purified histone H3 proteins. The amount of histone extracts for each assay can be 20 ng to 500 ng with an optimal range of 50 ng to 100 ng depending on the purity of histone extracts. The amount of purified histone H3 proteins for each assay can be 1 ng to 25 ng with an optimal range of 4 ng to 5 ng.

Fig. 3. Histone extracts were prepared from MCF-7 and MDA-231 cells using the EpiQuik™ Total Histone Extraction Kit (Cat. No. OP-0006) and multiple histone H3 modifications were screened and measured using the EpiQuik™ Histone H3 Modification Multiplex Assay Kit (Colorimetric). 100 ng of total histone proteins were used.

User Guide & MSDS

[User Guide]*
*Always use the actual User Guide that shipped with your product. Is the above file locked? You can also request user guides by emailing info@epigentek.com along with your contact information and institution name.

[Safety Data Sheet]
Product Citations

Al Sayed R et. al. (December 2019). A 2x folic acid treatment affects epigenetics and dendritic spine densities in SHSY5Y cells. Biochem Biophys Rep. 20:100681.

Gobert AP et. al. (October 2019). Bacterial Pathogens Hijack the Innate Immune Response by Activation of the Reverse Transsulfuration Pathway. MBio. 10(5)

Gambacurta A et. al. (June 2019). Human osteogenic differentiation in Space: proteomic and epigenetic clues to better understand osteoporosis. Sci Rep. 9(1):8343.

Bayo J et. al. (March 2019). A comprehensive study of epigenetic alterations in hepatocellular carcinoma identifies potential therapeutic targets. J Hepatol.

Peixoto P et. al. (February 2019). EMT is associated with an epigenetic signature of ECM remodeling genes. Cell Death Dis. 10(3):205.

Mukherjee K et. al. (February 2019). Epigenetic mechanisms mediate the experimental evolution of resistance against parasitic fungi in the greater wax moth Galleria mellonella. Sci Rep. 9(1):1626.

Zhou R et. al. (November 2018). Characterization of H3 methylation in regulating oocyte development in cyprinid fish. Sci China Life Sci.

Yang L et. al. (May 2018). Differential gene regulatory plasticity between upper and lower layer cortical excitatory neurons. Mol Cell Neurosci.

Parira T et. al. (September 2017). Novel detection of post-translational modifications in human monocyte-derived dendritic cells after chronic alcohol exposure: Role of inflammation regulator H4K12ac. Sci Rep. 7(1):11236.

Seth C et. al. (December 2016). Long-Lasting WNT-TCF Response Blocking and Epigenetic Modifying Activities of Withanolide F in Human Cancer Cells. PLoS One. 11(12):e0168170.

Bandyopadhaya A et. al. (October 2016). A quorum-sensing signal promotes host tolerance training through HDAC1-mediated epigenetic reprogramming. Nat Microbiol. 1:16174.

Lee HO et. al. (July 2016). Lack of global epigenetic methylation defects in CBS deficient mice. J Inherit Metab Dis.

Customer Reviews

Rating by n*****@health.missouri.edu Verified Purchase Reviewed on: Monday 05 June, 2017
Application Description
My experiment was to compare up to 21 histone H3 modifications in diseased and control rat testes. The input samples were total histone extracted from rat testes.

This product screens many histone modifications simultaneously which is time effective. I liked the extra strips for optimization as well as the controls included in the plate.

Because only 2 wells are available/treatment, using only 1 plate will not yield data for statistical analysis but rather a trend. You will need to purchase more than one plate which is costly to load at least 3 samples and end up with data that you can analyze with a statistical program.

Other Thoughts
How friendly was the user guide? (1 – worst, 5 – best) 5

How professional was the appearance and presentation of the product? (1 – worst, 5 – best) 5

The strips were very fragile and the wells broke apart when blotting the plate on paper towel to get rid of residual wash buffer. It will be nicer if they were sturdier.

20% Off m6A Antibodies
Related Products

Researchers Also Purchased
EpiQuik Total Histone Extraction Kit
EpiQuik Total Histone Extraction Kit
EpiQuik Histone H4 Modification Multiplex Assay Kit (Colorimetric)
EpiQuik Histone H4 Modification Multiplex Assay Kit (Colorimetric)
EpiQuik Total Histone Extraction HT Kit
EpiQuik Total Histone Extraction HT Kit
MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (Colorimetric)
MethylFlash Global DNA Methylation (5-mC) ELISA Easy Kit (Colorimetric)
Terms & Conditions | Privacy Policy | Site Map
Copyright © 2019 EpiGentek Group Inc. All rights reserved.