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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Mdm2 p53 binding protein homolog ( Mouse )
- 亚型:
IgG
- 形态:
liquid
- 保存条件:
负20摄氏度
- 克隆性:
Polyclonal antibody
- 标记物:
Non-conjugated
- 适应物种:
Human,Mouse ,Rat
- 保质期:
6个月
- 抗原来源:
Rabbit
- 目录编号:
P15248
- 级别:
纯化级别
- 库存:
50
- 供应商:
LSM bio
- 宿主:
E. coli - derived recombinant protein
- 应用范围:
ELISA,WB
- 浓度:
≥95% as determined by SDS-PAGE
- 靶点:
Mdm2 p53 binding protein homolog ( Mouse )
- 抗体英文名:
anti-MDM2 antibody,MDM2 antibody
- 抗体名:
anti-MDM2 抗体,MDM2 抗体
- 规格:
100μg
MDM2抗体| MDM2 antibody
货号 PAab05077
蛋白别名
蛋白介绍
E3 ubiquitin-protein ligase that mediates ubiquitination of p53/TP53, leading to its degradation by the proteasome. Inhibits p53/TP53- and p73/TP73-mediated cell cycle arrest and apoptosis by binding its transcriptional activation domain. Also acts as a ubiquitin ligase E3 toward itself and ARRB1. Permits the nuclear export of p53/TP53. Promotes proteasome-dependent ubiquitin-independent degradation of retinoblastoma RB1 protein. Inhibits DAXX-mediated apoptosis by inducing its ubiquitination and degradation. Component of the TRIM28/KAP1-MDM2-p53/TP53 complex involved in stabilizing p53/TP53. Also component of the TRIM28/KAP1-ERBB4-MDM2 complex which links growth factor and DNA damage response pathways. Mediates ubiquitination and subsequent proteasome degradation of DYRK2 in nucleus. Ubiquitinates IGF1R and SNAI1 and promotes them to proteasomal degradation.
产品描述
anti-MDM2 antibody is a Rabbit Polyclonal antibody againstMDM2..
建议稀释比例
IHC
Western blot
(本抗体仅供体外科研用途,不可用于临床诊断!) <"">
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文献和实验CELL杂志04年11月份的一篇paper,介绍了单个SNP的功能学研究的方法。 点击下面链接下载 A Single Nucleotide Polymorphism in the MDM2 Promoter Attenuates the p53 Tumor Suppressor Pathway and Accelerates Tumor Formation in Humans.pdf
小红赛 我目前在做药物靶向治疗肿瘤的课题,想在肿瘤细胞水平上以P53—MDM2为靶点,研究阻断MDM2或阻止P53水解时的信号变化及对细胞生长的影响,但目前不知道在P53—MDM2这个靶点上,有什么好的药物或者抑制剂,能用于细胞水平研究的,谢谢 selleckchem01 在这个靶点 下面两个抑制剂都可以用于细胞试验~ Nutlin-3 Nutlin-3 is a MDM
Antisense Oligonucleotide Inhibitors of MDM2 Oncogene Expression
Antisense therapy represents a novel genetic-based therapeutic approach, initiated by Zamecnik et al. about 20 years ago (1 ). The rationale for antisense oligonucleotide therapeutics is straightforward: to identify a specific inhibitor
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