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Merck
CN

SAB4200084

Sigma-Aldrich

Monoclonal Anti-AGO1 antibody produced in rat

~1 mg/mL, clone 4B8, purified immunoglobulin

别名:

Anti-Argonaute-1, Anti-Eukaryotic Translation Initiation Factor 2c, subunit 1, Anti-GERP95, Anti-Golgi Endoplasmic Reticulum protein 95 kDa

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关于此项目

UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

rat

偶联物

unconjugated

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

4B8, monoclonal

表单

buffered aqueous solution

分子量

antigen ~95 kDa

种属反应性

human, canine, mouse, monkey, bovine

浓度

~1 mg/mL

技术

immunoprecipitation (IP): suitable
western blot: 1-2 μg/mL using HEK-293T cell extracts

同位素/亚型

IgG2a

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... EIF2C1(26523)
mouse ... Eif2c1(236511)

一般描述

Monoclonal Anti-AGO1 (rat IgG2a isotype) is derived from the hybridoma 4B8 produced by the fusion of mouse myeloma cells (P3X63Ag8.653) and splenocytes from rat immunized with a recombinant human AGO1 fusion protein. The Argonaute family of proteins can be subdivided into the Ago subfamily and the Piwi subfamily. Argonaute proteins have a molecular weight of about 100 kDa and are characterized by piwi-argonaute-zwille (PAZ) and PIWI domains. In human, the Ago subfamily consists of hsAgo1−4 (also known as EIF2C1-4). Ago proteins localize to the cytoplasm of somatic cells and are concentrated in cytoplasmic processing bodies. A member of this group, Ago1 is also known to be associated with Golgi and with endoplasmic reticulum. The gene is located on chromosome 1. Eukaryotic initiation factor (EIF2C1)/hAgo1 is expressed in low to medium levels in most tissues, but its expression is particularly high in embryonic kidney and lung.

免疫原

recombinant human AGO1 fusion protein.

应用

  • Monoclonal Anti-AGO1 antibody produced in rat has been used in:
  • western blotting
  • immunoprecipitation
  • chromatin immunoprecipitation(CHIP) assay
  • RNA immunoprecipitation
  • RNA-nChIP experiments

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunoprecipitation (1 paper)

生化/生理作用

The Argonaute proteins are evolutionarily conserved between species and have been implicated in both transcriptional and post-transcriptional gene silencing. Eukaryotic initiation factor (EIF2C1)/argonaute 1 plays a vital role in activation of transcriptional enhancers and also regulates alternative splicing in human cells. EIF2C1 levels are also increased in tumors that lack the Wilm′s tumor suppressor gene WT1.The encoded protein interacts with hypoxia-responsive microRNAs (HRMs) and stimulate angiogenic pathway.

外形

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

10 - Combustible liquids

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Michaela Beitzinger et al.
RNA biology, 4(2), 76-84 (2007-07-20)
MicroRNAs (miRNAs) constitute a class of small non-coding RNAs that regulate gene expression on the level of translation and/or mRNA stability. Mammalian miRNAs associate with members of the Argonaute (Ago) protein family and bind to partially complementary sequences in the
Argonaute proteins couple chromatin silencing to alternative splicing
Ameyar-ZM, et al.
Nature Structural and Molecular Biology, 19(10), 998-998 (2012)
RNA activating-double stranded RNA targeting flt-1 promoter inhibits endothelial cell proliferation through soluble FLT-1 upregulation
Choi S, et al.
Testing, 13(3), e0193590-e0193590 (2018)
Hypoxia-responsive miRNAs target argonaute 1 to promote angiogenesis
Chen Z, et al.
The Journal of Clinical Investigation, 123(3), 1057-1057 (2013)
Argonaute protein as a linker to command center of physiological processes
Wei K, et al.
Chinese Journal of Cancer Research = Chung-kuo Yen Cheng Yen Chiu, 25(4), 430-430 (2013)

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