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HDAC8 deacetylase substrate 荧光 组蛋白去乙酰化酶8 二乙酰化多肽底物
526 人阅读发布时间：2015-06-12 11:17
FLUOR DE LYS®-HDAC8 deacetylase substrate BML-KI178-0005
荧光 组蛋白去乙酰化酶8 二乙酰化多肽底物
纯度 95%
保存 -80度
状态 5 mM溶液 (100 ul )
文献引用
Compromised Structure and Function of HDAC8 Mutants Identified in Cornelia de Lange Syndrome Spectrum Disorders: C. Decroos, et al.; ACS Chem. Biol. 9, 2157 (2014), Application(s): Assay of human HDAC8, Abstract;
Molecular Basis for the Antiparasitic Activity of a Mercaptoacetamide Derivative That Inhibits Histone Deacetylase 8 (HDAC8) from the Human Pathogen Schistosoma mansoni: D. Stolfa, et al.; J. Mol. Biol. 426, 3442 (2014), Application(s): In vitro HDAC inhibition assay of parasitic flatworm, Abstract;
Structural basis for the inhibition of histone deacetylase 8 (HDAC8), a key epigenetic player in the blood fluke Schistosoma mansoni: M. Marek, et al.; PLoS Pathog. 9, e1003645 (2013), Application(s): Human and smHDAC8 activity assay, Abstract;Full Text
Insights from comprehensive multiple receptor docking to HDAC8: M. Brunsteiner, et al.; J. Mol. Model. 18, 3927 (2012),Abstract;
荧光 组蛋白去乙酰化酶8 二乙酰化多肽底物
纯度 95%
保存 -80度
状态 5 mM溶液 (100 ul )
| 货号 | 产品名称 | 规格 | 中文名称 | 品牌 |
| BML-KI178-0005 | FLUOR DE LYS® - HDAC8 deacetylase substrate | 0.5 umol | 荧光 组蛋白去乙酰化酶8 二乙酰化多肽底物 |
ENZO(美国) |
文献引用
Compromised Structure and Function of HDAC8 Mutants Identified in Cornelia de Lange Syndrome Spectrum Disorders: C. Decroos, et al.; ACS Chem. Biol. 9, 2157 (2014), Application(s): Assay of human HDAC8, Abstract;
Molecular Basis for the Antiparasitic Activity of a Mercaptoacetamide Derivative That Inhibits Histone Deacetylase 8 (HDAC8) from the Human Pathogen Schistosoma mansoni: D. Stolfa, et al.; J. Mol. Biol. 426, 3442 (2014), Application(s): In vitro HDAC inhibition assay of parasitic flatworm, Abstract;
Structural basis for the inhibition of histone deacetylase 8 (HDAC8), a key epigenetic player in the blood fluke Schistosoma mansoni: M. Marek, et al.; PLoS Pathog. 9, e1003645 (2013), Application(s): Human and smHDAC8 activity assay, Abstract;Full Text
Insights from comprehensive multiple receptor docking to HDAC8: M. Brunsteiner, et al.; J. Mol. Model. 18, 3927 (2012),Abstract;