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SET7/9 (human), (recombinant)

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Histone methyltransferase that transfers methyl groups to Lys⁴ of histone H3, in complex with S-adenosyl-L-methionine.

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Alternative Name	Histone H3-K4 methyltransferase
Concentration	1mg/ml
Endotoxin Content	<1.0EU/µg protein (LAL test)
Formulation	Liquid. In 50mM TRIS-HCl, pH 7.5, containing 0.2M sodium chloride, 5mM DTT and 20% glycerol.
MW	~40.7kDa.
Purity	≥95% (SDS-PAGE)
Source	Produced in E. coli.
UniProt ID	Q8WTS6

Regulatory Status	RUO – Research Use Only

Identification and Characterizations of Novel, Selective Histone Methyltransferase SET7 Inhibitors by Scaffold Hopping- and 2D-Molecular Fingerprint-Based Similarity Search: H. Ding, et al.; Molecules 23, E567 (2018), Abstract — Full Text
Miniaturization of High-Throughput Epigenetic Methyltransferase Assays with Acoustic Liquid Handling: B. Edwards, et al.; J. Lab. Autom. 21, 208 (2016), Abstract
Modulations of DNA Contacts by Linker Histones and Post-translational Modifications Determine the Mobility and Modifiability of Nucleosomal H3 Tails: A. Stutzer, et al.; Mol. Cell 61, 247 (2016), Abstract
Development of homogeneous nonradioactive methyltransferase and demethylase assays targeting histone H3 lysine 4: N. Gauthier, et al.; J. Biomol. Screen. 17, 49 (2012), Abstract
Effects of a novel arginine methyltransferase inhibitor on T-helper cell cytokine production: K. Bonham, et al.; FEBS J. 277, 2096 (2010), Abstract — Full Text
Mechanism of histone lysine methyl transfer revealed by the structure of SET7/9-AdoMet: T. Kwon, et al.; EMBO J. 22, 292 (2003), Abstract

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