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Merck
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文件

07-539

Sigma-Aldrich

抗乙酰组蛋白H3(Lys4)抗体

Upstate®, from rabbit

别名:

H3K4Ac, Histone H3 (acetyl K4)

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

rabbit

品質等級

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

純化經由

affinity chromatography

物種活性

human

製造商/商標名

Upstate®

技術

ChIP: suitable (ChIP-seq)
dot blot: suitable
inhibition assay: suitable (peptide)
multiplexing: suitable
western blot: suitable

同型

IgG

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

acetylation (Lys 4)

基因資訊

human ... H3F3B(3021)

特異性

组蛋白H3在Lys4上乙酰化时
预计具有广泛的物种交叉反应性

免疫原

KLH偶联合成肽包含序列 ...RT[AcK]Q...,其中[AcK]对应于人组蛋白H3的乙酰赖氨酸4

應用

建议的稀释度:
蛋白质印迹:1:1000 - 1:10,000
抗乙酰基组蛋白H3(Lys 4)抗体是一种兔多克隆抗体,用于检测乙酰基组蛋白H3(Lys 4),也称为H3K4Ac,组蛋白H3(乙酰基K4)& 已在Mplex、WB、PIA、ChIP、ChIP-seq、DB中得到验证。
研究子类别
组蛋白
研究类别
表观遗传学&核功能

品質

已通过免疫印迹进行常规评估。

標靶描述

Mr ~17kDa

外觀

100 μL免疫亲和纯化的兔IgG,溶于在含有0.1 M Tris-甘氨酸(pH 7.4)和0.15 M NaCl,并含有0.05%叠氮化钠和30%甘油的缓冲液中
免疫亲和纯化

儲存和穩定性

自运送之日起在-20°C下保存1年

法律資訊

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

免責聲明

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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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1


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Epigenetic regulation of chromatin plays a critical role in controlling embryonic stem (ES) cell self-renewal and pluripotency. However, the roles of histone demethylases and activating histone modifications such as trimethylated histone 3 lysine 4 (H3K4me3) in transcriptional events such as
Federico Forneris et al.
The Journal of biological chemistry, 281(46), 35289-35295 (2006-09-22)
Human lysine-specific demethylase (LSD1) is a chromatin-modifying enzyme that specifically removes methyl groups from mono- and dimethylated Lys4 of histone H3 (H3-K4). We used a combination of in vivo and in vitro experiments to characterize the substrate specificity and recognition
Cheng-Yu Yang et al.
Oncotarget, 8(20), 33756-33769 (2017-04-20)
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The Journal of biological chemistry, 291(9), 4523-4536 (2016-01-07)
Inhibiting class I histone deacetylases (HDACs) increases energy expenditure, reduces adiposity, and improves insulin sensitivity in obese mice. However, the precise mechanism is poorly understood. Here, we demonstrate that HDAC1 is a negative regulator of the brown adipocyte thermogenic program.
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