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Merck
CN
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文件

04-642

Sigma-Aldrich

抗Ago2抗体,克隆9E8.2

ascites fluid, clone 9E8.2, Upstate®

别名:

Argonaute-2, Eukaryotic translation initiation factor 2C, AGO2, eIF-2C, Slicer protein, MGC3183, Piwi domain protein, PPD

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About This Item

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

生物来源

mouse

质量水平

抗体形式

ascites fluid

抗体产品类型

primary antibodies

克隆

9E8.2, monoclonal

种属反应性

human

制造商/商品名称

Upstate®

技术

ChIP: suitable (ChIP-seq)
western blot: suitable

同位素/亚型

IgG1κ

NCBI登记号

UniProt登记号

运输

wet ice

靶向翻译后修饰

unmodified

基因信息

human ... AGO2(27161)

一般描述

Ago2(argonaute-2),也称为真核翻译起始因子2C(EIF2C2),是siRNA定向RNA干扰(RNAi)反应的重要组成部分。 Ago2是解开siRNA双链体和将siRNA组装成RNA诱导的沉默复合物(RISC)所需的核酸内切酶。 Ago2通过其Piwi域与DICER1相互作用。 该Piwi结构域被认为通过类似于RNase H的机制提供RNA切割活性。Ago2活性对于胚胎发育以及RNA介导的基因沉默(RNAi)是必需的。

特异性

人Ago2

免疫原

KLH偶联的合成肽,包含序列YSGAGPALAPPAPPPPIQG
表位:在Ago2的N端附近

应用

ChIP和ChIP-seq:该抗体的代表性批次用于执行ChIP和ChIP-seq(Woolnough, JL, Atwood, BL, and Giles KE (2015), MCB Vol. 35 No. 13, p. 2278-2294)。
抗Ago2抗体,克隆9E8.2是一种小鼠单克隆抗体,用于检测Ago2(也称为Argonaute-2,真核翻译起始因子2C),&已在WB中验证,并已证明可在ChIP和ChIP-seq中执行。
研究子类别
RNA代谢&结合蛋白

染色质生物

RNA结合蛋白(RBP)
研究类别
表观遗传学&核功能

质量

已通过免疫印迹进行常规评估。

目标描述

~100 kda

外形

免疫亲和纯化
含0.05%叠氮化钠的腹水

储存及稳定性

自收到之日起,在-20°C条件下可稳定保存1年。
处理建议:收到后,在取下瓶盖之前,将小瓶离心并轻轻混合溶液。分装到微量离心管中,并储存于 -20°C。避免反复冻融循环,以免损坏IgG和影响产品性能

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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WGK

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闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Keriayn N Smith et al.
Stem cell reports, 9(1), 108-121 (2017-06-06)
Of the thousands of long noncoding RNAs expressed in embryonic stem cells (ESCs), few have known roles and fewer have been functionally implicated in the regulation of self-renewal and pluripotency, or the reprogramming of somatic cells to the pluripotent state.
Li Zhang et al.
Cell death & disease, 10(3), 168-168 (2019-02-20)
Cholestasis induces the hepatic long non-coding RNA H19, which promotes the progression of cholestatic liver fibrosis. However, microRNAs that are dysregulated by H19 during cholestasis remain elusive. Using miRNA-sequencing analysis followed by qPCR validation, we identified marked upregulation of eight
Simon J Allison et al.
Molecular therapy. Nucleic acids, 2, e141-e141 (2014-01-09)
Selective gene silencing by RNA interference (RNAi) involves double-stranded small interfering RNA (ds siRNA) composed of single-stranded (ss) guide and passenger RNAs. siRNA is recognized and processed by Ago2 and C3PO, endonucleases of the RNA-induced silencing complex (RISC). RISC cleaves
Differential expression of microRNA expression in tamoxifen-sensitive MCF-7 versus tamoxifen-resistant LY2 human breast cancer cells.
Manavalan, TT; Teng, Y; Appana, SN; Datta, S; Kalbfleisch, TS; Li, Y; Klinge, CM
Cancer letters null
Song Chen et al.
Experimental and therapeutic medicine, 22(4), 1049-1049 (2021-08-27)
Sepsis is a condition that is associated with high rates of mortality. It is characterized by serious systemic inflammatory responses induced by pathogenic invasion. Although microRNA-150 (miR-150) has been previously reported to be involved in the modulation of sepsis, the

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