Anti-Human/Mouse SETD2 Polyclonal Antibody

SETD2多克隆抗体

Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein belonging to a class of huntingtin interacting proteins characterized by WW motifs. This protein is a histone methyltransferase that is specific for lysine-36 of histone H3, and methylation of this residue is associated with active chromatin. This protein also contains a novel transcriptional activation domain and has been found associated with hyperphosphorylated RNA polymerase II.
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基本信息

数据文档 查看数据文档
货号 PA12831
规格 100μl
宿主 Rabbit
免疫原 Recombinant protein of human SETD2
特异性 Ubiquitously expressed.
亚型 IgG
反应性 Human,Mouse
克隆
Uniprot Q9BYW2
浓度 0.2 mg/mL
推荐稀释度 IHC 1:50-1:200
配方
应用范围 IHC,ELISA
别名 EC 2.1.1.43,FLJ16420,FLJ22472,FLJ23184,FLJ45883,HBP231,HIF 1,HIF-1,HIF1,HIP-1,Histone lysine N methyltransferase SETD2,Histone-lysine N-methyltransferase SETD2,hSET2,HSPC069,Huntingtin interacting protein 1,Huntingtin interacting protein,Huntingtin interacting protein B,Huntingtin interacting protein HYPB,Huntingtin yeast partner B,Huntingtin-binding protein,231-KD,Huntingtin-interacting protein 1,Huntingtin-interacting protein B,HYPB,KIAA1732,KMT3A,Lysine N methyltransferase 3A,Lysine N-methyltransferase 3A,p231HBP,SET domain containing 2,SET domain-containing protein 2,SET2,SETD2,SETD2
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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