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主要文件

04-1530

Sigma-Aldrich

抗MDM2抗体,克隆3G9

clone 3G9, from mouse

别名:

Double minute 2 protein, Mdm2 p53 binding protein homolog (mouse), Mdm2, transformed 3T3 cell double minute 2, p53 binding protein, Mdm2, transformed 3T3 cell double minute 2, p53 binding protein (mouse), Oncoprotein Mdm2, double minute 2, human homolog

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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

purified antibody

抗体产品类型

primary antibodies

克隆

3G9, monoclonal

种属反应性

human

种属反应性(根据同源性预测)

mouse (based on 100% sequence homology)

包装

antibody small pack of 25 μL

技术

immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

NCBI登记号

UniProt登记号

运输

ambient

靶向翻译后修饰

unmodified

基因信息

human ... MDM2(4193)
mouse ... Mdm2(17246)

一般描述

MDM2在许多肿瘤中过表达。它的主要功能是p53抑癌蛋白的泛素化和降解。当Thr-216未被磷酸化时,该单克隆抗体还可识别鼠MDM2的Thr-216周围的肽表位。SMP14还可与某些细胞角蛋白(6、14 & 16)发生交叉反应。这仅在处理某些上皮细胞时会产生此问题,而成纤维细胞不会。

特异性

该抗体可识别MDM2。

免疫原

带His标签的重组蛋白,对应于人MDM2。
表位:未知

应用

免疫沉淀分析: 一个代表性批次已在一个独立实验室中进行此应用。(Changgong, L., et al. (2002). Molecular and Cellular Biology.22(21):7562-7571.)
抗MDM2抗体,克隆3G9,是一种小鼠单克隆抗体,可用于检测MDM2(也称为双微2蛋白或Mdm2 p53结合蛋白同源物) &,其已通过WB、IP、ICC、&IHC验证。
研究子类别
RNA代谢 & 结合蛋白

泛素 & 泛素代谢
研究类别
表观遗传学&核功能

质量

通过蛋白质印迹对MCF-7细胞裂解液进行了评估。

蛋白质印迹分析:0.5 µg/ml该抗体可在10 µg的MCF-7细胞裂解液中检测到MDM2。

目标描述

~75 kDa

外形

形式:纯化
纯化的小鼠单克隆IgGκ,溶于含有0.1 M Tris-甘氨酸(pH 7.4,150 mM NaCl)和0.05%叠氮化钠的缓冲液中。
蛋白G纯化

储存及稳定性

自发运之日起,在 2-8°C 条件下可稳定保存1年

分析说明

对照
MCF-7细胞裂解液

其他说明

浓度:请参考批次特异性浓缩物的分析证书。

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 1

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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访问文档库

Zhenzhen Liu et al.
Chemical biology & drug design, 85(4), 411-417 (2014-09-18)
In this article, we describe a no-wash small-molecule fluorescent probe for detecting and imaging p53-MDM2 protein-protein interaction based on an environment-sensitive fluorescent turn-on mechanism. After extensive biological examination, this probe L1 exhibited practical activity and selectivity in vitro and in
Zhuohao Liu et al.
Diabetes, 67(11), 2397-2409 (2018-08-23)
Profound loss and senescence of adipose tissues are hallmarks of advanced age, but the underlying cause and their metabolic consequences remain obscure. Proper function of the murine double minute 2 (MDM2)-p53 axis is known to prevent tumorigenesis and several metabolic
Xiaomu Li et al.
Nature communications, 7, 11740-11740 (2016-06-07)
Mitochondrial metabolism is pivotal for glucose-stimulated insulin secretion (GSIS) in pancreatic β-cells. However, little is known about the molecular machinery that controls the homeostasis of intermediary metabolites in mitochondria. Here we show that the activation of p53 in β-cells, by
Lenka Kyjacova et al.
Oncogene, 40(47), 6494-6512 (2021-10-07)
Expression of the immediate-early response gene IER2 has been associated with the progression of several types of cancer, but its functional role is poorly understood. We found that increased IER2 expression in human melanoma is associated with shorter overall survival
Ting Ni et al.
Nature cell biology, 18(11), 1221-1232 (2016-10-28)
The zinc-finger transcription factor Snail1 is inappropriately expressed in breast cancer and associated with poor prognosis. While interrogating human databases, we uncovered marked decreases in relapse-free survival of breast cancer patients expressing high Snail1 levels in tandem with wild-type, but

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