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Histone 3 is a nuclear protein and a component of the nucleosome core, a basic unit of chromatin, that is essential for organizing genomic DNA in eukaryotic nuclei.1 It is a globular protein that contains a histone fold domain with a C-terminal α-helix that facilitates nucleosome interactions and chromatin compaction, as well as an unstructured N-terminal tail that extends outside of the nucleosome core, both of which are subject to various post-translational modifications (PTMs), including ubiquitination, acetylation, methylation, and phosphorylation.1,2,3 Histone H3 has a key role in transcriptional regulation.4 A lysine-to-methionine mutation at residue 36 in histone H3.3 (H3.3K36M) is associated with chondroblastomas.5 Cayman’s Histone H3K36M Rabbit Monoclonal Antibody - Biotinylated (Clone RM193) can be used for chromatin immunoprecipitation (ChIP), ELISA, immunohistochemistry (IHC), and Western blot (WB) applications.
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1. Writing, erasing and reading histone lysine methylations. Exp. Mol. Med. 49(4), e324 (2017).
2. The role of histone H2A and H2B post-
3. The C-
4. Covalent modifications of histones during development and disease pathogenesis. Nat. Struct. Mol. Biol. 14(11), 1008-1016 (2007).
5. The histone H3.3K36M mutation reprograms the epigenome of chondroblastomas. Science 352(6291), 1344-1348 (2016).