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Merck
CN

04-642

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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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

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)

相关类别

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。
~100 kda

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

生化/生理作用

人Ago2

外形

免疫亲和纯化
含0.05%叠氮化钠的腹水

制备说明

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

分析说明

已通过免疫印迹进行常规评估。

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

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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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
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.
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
Hanane Ennajdaoui et al.
Cell reports, 15(9), 1876-1883 (2016-05-24)
Insulin-like growth factor 2 mRNA binding protein 3 (IGF2BP3) expression correlates with malignancy, but its role(s) in pathogenesis remains enigmatic. We interrogated the IGF2BP3-RNA interaction network in pancreatic ductal adenocarcinoma (PDAC) cells. Using a combination of genome-wide approaches, we have

相关内容

All eukaryotic organisms require tight regulation of gene expression for complex processes such as development, differentiation, cell specification, and responses to environmental stimuli. Many genes are regulated post-transcriptionally, in addition to transcriptional mechanisms of gene regulation. RNA-binding proteins (RBPs) are essential for post-transcriptional gene regulation, linking transcription and translation in many processes including transcription, splicing, export, rate of translation and turnover. In all of these events, RBPs coordinate regulation of the amount of protein produced from mRNA transcripts.

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