A comprehensive and unbiased map of histone post-translational modifications (PTMs) is the cornerstone of modern epigenetic discovery, revealing the molecular logic behind gene regulation, cellular identity, and disease. CD BioSciences addresses this foundational need with our advanced histone PTM profiling service. Leveraging high-resolution mass spectrometry and integrated bioinformatics, we provide researchers with a powerful, antibody-independent platform to quantitatively decode the complete histone modification landscape.
Histone post-translational modifications (PTMs) constitute a complex and dynamic molecular language that dictates chromatin structure and function, with direct implications for gene regulation, development, and disease. Profiling these modifications at a systems level is therefore critical; however, traditional antibody-based methods are inherently limited in scope and bias. Histone PTM profiling using high-resolution mass spectrometry provides an unbiased, quantitative, and comprehensive approach to decode this epigenetic landscape. This service enables the discovery of novel modifications, the precise mapping of modification crosstalk, and the systematic identification of disease-associated PTM signatures, forming an essential foundation for hypothesis generation and mechanistic follow-up in modern chromatin biology.

Fig.1 Histone post-translational modifications (PTMs) in chromosome condensation. (Andonegui-Elguera M A, et al., 2022)
As a leading provider of integrated epigenetic research services, CD BioSciences offers a professional histone PTM profiling service designed to translate complex biological samples into actionable epigenetic insights. We leverage advanced, high-resolution mass spectrometry platforms coupled with expert bioinformatic analysis to deliver comprehensive, quantitative maps of histone modifications. Our service transforms raw spectral data into clear biological narratives, identifying differential PTM signatures and revealing the epigenetic underpinnings of your experimental conditions, disease states, or developmental processes.
Our service is built upon a high-resolution, high-sensitivity LC-MS/MS platform, enabling unbiased and quantitative analysis of a broad spectrum of histone post-translational modifications (PTMs). This powerful technology allows for the precise detection, relative quantification, and site-specific mapping of diverse modifications, including but not limited to methylation, acetylation, phosphorylation, diverse acylations, ubiquitination, and glycosylation, providing a panoramic view of the epigenetic landscape.
| Service | Specific Targets & Notes |
|---|---|
| Histone Lysine/Arginine Methylation Analysis | Mono-, Di-, Tri-methylation on lysine; Mono- & Di-methylation (symmetric/asymmetric) on arginine. |
| Histone Lysine Acetylation Analysis | Identification and quantification of acetylated lysine residues. |
| Histone Lysine Acylation Analysis | Broad detection of various short-chain acylations (e.g., propionylation, butyrylation). |
| Histone Lysine Crotonylation Analysis | Specific analysis for the crotonyllysine mark. |
| Histone Lysine Lactylation Analysis | Specific analysis for the lactyllysine mark. |
| Histone Lysine Formylation Analysis | Specific analysis for formyllysine. |
| Histone Lysine Ubiquitination Analysis | Detection of mono-ubiquitination marks (requires specific sample preparation/enrichment). |
| Histone Lysine SUMOylation Analysis | Detection of SUMOylation marks (requires specific sample preparation/enrichment). |
| Histone Serine/Threonine/Tyrosine Phosphorylation Analysis | Mapping of phosphorylation sites on serine, threonine, and tyrosine residues. |
| Histone Arginine Citrullination Analysis | Detection of citrullination (deimination) on arginine residues. |
| Histone Serine/Threonine O-GlcNAcylation Analysis | Analysis of O-linked N-acetylglucosamine modification (requires specific enrichment strategies). |
*This list represents our core analytical capabilities. We also support customized targeted analysis for specific modification panels and discovery-driven global profiling to identify novel or unexpected PTM changes.
The basic principle for the identification of histone post-translational modification by mass spectrometry is the change of molecular weight before and after modification. Compared with histones that have not been modified, histones suffered with PTMs hold increased molecular weight at a particular sequence. PTMs of histone can be detected by high-precision mass spectrometry that can distinguish the changes of molecular weight, to further confirm modification type and site. Therefore, as long as we know the precise changes of molecular weight before and after modification, we can help you to identify any histone PTMs.

Fig.2 Workflow of histone PTMs identification.
Supported Sample Types
Diverse Application Scenarios
Deciphering the histone code requires robust, unbiased, and quantitative tools. At CD BioSciences, our histone PTM profiling service delivers precisely that, transforming your complex biological samples into clear, actionable epigenetic insights through high-resolution mass spectrometry and expert analysis. This service not only maps the existing landscape but also opens doors to novel discoveries, providing a critical data foundation for the next generation of chromatin research. If you are interested in our services, please feel free to contact us for more details and quotation information of related services.
Reference
1. Andonegui-Elguera M A, Cáceres-Gutiérrez R E, López-Saavedra A, et al. The roles of histone post-translational modifications in the formation and function of a mitotic chromosome[J]. International Journal of Molecular Sciences, 2022, 23(15): 8704.
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