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Merck
CN

05-678

抗泛素组蛋白H2A抗体,克隆E6C5

clone E6C5, Upstate®, from mouse

别名:

H2AUb, Histone H2A (ubiquityl), H2A histone family, member R, histone 1, H2aa, histone H2A, histone cluster 1, H2aa, H2AK119Ub1

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关于此项目

UNSPSC代码:
12352203
eCl@ss:
32160702
NACRES:
NA.41
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生物来源

mouse

质量水平

偶联物

unconjugated

抗体形式

purified antibody

抗体产品类型

primary antibodies

克隆

E6C5, monoclonal

种属反应性

amphibian, mouse, human, frog, rat, monkey

制造商/商品名称

Upstate®

技术

ChIP: suitable
immunocytochemistry: suitable
western blot: suitable

同位素/亚型

IgM

NCBI登记号

UniProt登记号

运输

dry ice

靶向翻译后修饰

unmodified

基因信息

frog ... H2Ac1(594915)
human ... H2AC1(221613)
mouse ... H2Ac1(319163)
rat ... H2Ac1(24828)

一般描述

25 kDa
组蛋白是高度保守的蛋白质,可作为将核DNA组织成染色质的结构支架。组蛋白在翻译后通过乙酰化、磷酸化、甲基化和泛素化进行修饰,这些修饰调节DNA转录、修复、重组和复制。泛素化通常靶向降解的底物,尽管组蛋白H2A和H2B实际上通过单个泛素结合而稳定。 组蛋白泛素化与DNA修复和转录,细胞分化,细胞周期调控,精子发生,蛋白质运输以及对压力的反应有关。 组蛋白H2A在Lys119处被PRC-1L复合物(Polycomb repressive complex 1-like)单泛素化,该复合物包括Ring1,Ring2,Bmi1和HPH2。 泛素化的H2A通常占H2A的约15%,但在活性染色质中该值可高达50%。 泛素化组蛋白H2A也与大染色质区域的转录沉默有关,并与Polycomb沉默有关,因此泛素化H2A的功能仍然不确定。

免疫原

AMA(人上皮羊膜)细胞残留核团部分。

应用

使用抗泛素-组蛋白H2A抗体,克隆E6C5(小鼠单克隆抗体)已发表并经验证可用于ChIP、ICC、WB,以检测泛素-组蛋白H2A(也称为H2AUb、组蛋白H2A(泛素)、组蛋白H2A)。
免疫细胞化学:
该抗体已由独立实验室报告用于检测用3%甲醛/0.1% Triton X-100或甲醇固定的细胞中的泛素组蛋白H2A(Vassilev,A.1995)。

染色质免疫沉淀:
由独立实验室报告(Wang, H. 2004)。
研究子类别
组蛋白
研究类别
表观遗传学&核功能

生化/生理作用

不与粘虫发生交叉反应。
其他物种还未经测试。
该抗体识别并特异于单泛素组蛋白H2A(Lys119),Mr~25 kDa。

外形

形式:纯化
纯化的小鼠单克隆IgM溶于缓冲液(含0.05%叠氮化钠的PBS)中,然后添加甘油至30%。在-20ºC为液体形式。

制备说明

自收到之日起在-20°C可稳定保存1年。 为了最大程度地回收产品,在取下盖子之前,将原始样品瓶进行离心。

分析说明

对照
HeLa细胞的酸提取物
通过蛋白质印迹法对HeLa和10T1/2细胞的酸提取物中的H2A进行了常规评估。

蛋白质印迹分析:
该批次以1:500-1:2000的稀释度在HeLa和10T1/2细胞的酸提取物中检测到泛素组蛋白H2A。

其他说明

浓度:请参考批次特异性浓缩物的分析证书。

法律信息

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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在文件库中查找您最近购买产品的文档。

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Qin Li et al.
Carcinogenesis, 30(7), 1243-1251 (2009-04-21)
In the present study, we examined the effects of CoCl(2) on multiple histone modifications at the global level. We found that in both human lung carcinoma A549 cells and human bronchial epithelial Beas-2B cells, exposure to CoCl(2) (>/=200 muM) for
Yanlai Lai et al.
Archives of biochemistry and biophysics, 518(2), 103-110 (2012-01-12)
Inactivation of the von Hippel-Lindau (VHL) tumor suppressor is associated with renal carcinoma, hemangioblastoma and pheochromocytoma. The VHL protein is a component of a ubiquitin ligase complex that ubiquitinates and degrades hypoxia inducible factor-α (HIF-α). Degradation of HIF-α by VHL
Genome-wide uH2A localization analysis highlights Bmi1-dependent deposition of the mark at repressed genes.
Kallin, EM; Cao, R; Jothi, R; Xia, K; Cui, K; Zhao, K; Zhang, Y
PLoS Genetics null
Andreas K Hock et al.
The Journal of biological chemistry, 289(50), 34862-34870 (2014-10-23)
Ubiquitin-specific peptidase 42 (USP42) is a deubiquitylating enzyme that can target p53 and contribute to the stabilization of p53 in response to stress. We now show that USP42 can also regulate transcription independently of p53. USP42 co-localized with RNA polymerase
Alexander Krichevsky et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(27), 11157-11162 (2011-06-22)
Covalent modifications of histones, such as acetylation, methylation and ubiquitination, are central for regulation of gene expression. Heterochromatic gene silencing, for example, is associated with hypoacetylation, methylation and demethylation, and deubiquitination of specific amino acid residues in histone molecules. Many

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