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ab31865 has been referenced in 5 publications.
Brideau NJ et al.
Independent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome.
Mol Cell Biol 35:4053-68 (2015).
Massah S et al.Epigenetic characterization of the growth hormone gene identifies SmcHD1 as a regulator of autosomal gene clusters.PLoS One 9:e97535 (2014).
Tang M et al.Structural maintenance of chromosomes flexible hinge domain containing 1 (SMCHD1) promotes non-homologous end joining and inhibits homologous recombination repair upon DNA damage.J Biol Chem 289:34024-32 (2014).
Lemmers RJ et al.Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2.Nat Genet 44:1370-4 (2012).
Nikolov M et al.Chromatin affinity purification and quantitative mass spectrometry defining the interactome of histone modification patterns.Mol Cell Proteomics 10:M110.005371 (2011).
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