Histone H3 (21-44)

Names

[ Name ]:
Histone H3 (21-44)

Biological Activity

[Description]:

Histone H3 (21-44), derived from histone H3 21-44 amino acids, is usually used as a substrate (such as protein arginine methyltransferases) for methylation assays[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[References]

[1]. Santos-Rosa H, Caldas C. Chromatin modifier enzymes, the histone code and cancer. Eur J Cancer. 2005;41(16):2381-2402.

Chemical & Physical Properties

[ Molecular Formula ]:
C₁₀₉H₁₈₅N₃₉O₂₉

[ Molecular Weight ]:
2505.91

Related Compounds

(Lys(Me)3²⁷)-Histone H3 (21-44)-Gly-Lys(biotinyl) trifluoroacetate salt
Histone H3 (1-21)
Histone H3 (1-25), amide
Histone H3 (1-20) trifluoroacetate salt
Histone H3 (5-23)
Histone H3 (23-34)
2-((1-(3-chlorophenyl)-5-phenyl-1H-imidazol-2-yl)thio)-N-phenylacetamide
2-((1-(4-fluorophenyl)-5-(3-nitrophenyl)-1H-imidazol-2-yl)thio)-N-methylacetamide
3U7Vfb9zjg
(9E,11E,13S)-13-Hydroperoxyoctadeca-9,11-dienoic acid
5-(4-bromophenyl)-1-(4-fluorophenyl)-2-(methylthio)-1H-imidazole
5-(4-bromophenyl)-2-(ethylthio)-1-(4-fluorophenyl)-1H-imidazole
2-((5-(4-bromophenyl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)thio)acetonitrile
4-(4-methylpiperazin-1-yl)-N-[5-(4-phenylmethoxyphenoxy)-1H-indazol-3-yl]benzamide
4-(4-methylpiperazin-1-yl)-N-[5-(3-phenylmethoxyphenoxy)-1H-indazol-3-yl]benzamide
4-(4-methylpiperazin-1-yl)-N-[5-(4-phenoxyphenoxy)-1H-indazol-3-yl]benzamide