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抗 WWP2 磁珠
蛋白与多肽

抗 WWP2 磁珠

02AB00103

WWP2 (WW Domain Containing E3 Ubiquitin Protein Ligase 2) is an E3 ubiquitin ligase that plays a crucial role in various biological processes, including protein ubiquitination, chondrogenesis, and oncogenic signaling pathways. It interacts with Smad proteins and the tumor suppressor PTEN, influencing cell signaling and differentiation. WWP2 has been linked to several diseases, including Spondyloepiphyseal Dysplasia, Nishimura Type, and Cowden Syndrome 1, and its dysregulation can contribute to fibrosis, inflammation, and cancer progression. The inhibition of WWP2 has been identified as a potential therapeutic strategy for treating diseases characterized by fibrosis and inflammation, as it regulates the expression of pro-inflammatory factors and fibroblast activation. Additionally, WWP2 isoforms have distinct functions, with WWP2-N potentially suppressing TGFβ-induced epithelial-to-mesenchymal transition (EMT) and WWP2-C interacting with inhibitory Smad7.

Human
规格起售价
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技术参数

宿主
Mouse
靶点基因名
WWP2
蛋白别名
WW domain containing E3 ubiquitin protein ligase 2; WWP2
UniProt
O00308
物种
Human
应用
IP
Monoclonal
IgG2a

产品详情

靶点名称
WWP2
蛋白名称
WW domain containing E3 ubiquitin protein ligase 2
蛋白别名
NEDD4-like E3 ubiquitin-protein ligase WWP2; Atrophin-1-interacting protein 2; AIP2; HECT-type E3 ubiquitin transferase WWP2; WW domain-containing protein 2
靶点基因名
WWP2
UniProt
O00308
来源物种
Homo sapiens (Human)
宿主物种
Mouse
物种反应性
Human
克隆性
Monoclonal
亚型
IgG2a
配方
Supplied as solution in phosphate buffered saline containing 0.1% BSA and 0.02% sodium azide
剂型
Subject to solid-liquid separation upon standing; Mix thoroughly to ensure a consistent, homogeneous

免疫原核心序列

TAVAPENRHQPPSTNCFGGRSRTHRHSGASARTTPATGEQSPGARSRHRQPVKNSGHSGLANGTVNDEPTTATDPEEPSVVGVTSPPAAPLSVTPNPNTTSLPAPATPAEGEEPSTSGTQQLPAAAQAPDALPAGWEQRELPNGRVYYVDHNTKTTTWERPLPPGWEKRTDPRGRFYYVDHNTRTTTWQRPTAEYVRNYE

应用推荐稀释比备注
IP—50-100 μL/200 μg cell lysate

背景介绍

WWP2 (WW Domain Containing E3 Ubiquitin Protein Ligase 2) is an E3 ubiquitin ligase that plays a crucial role in various biological processes, including protein ubiquitination, chondrogenesis, and oncogenic signaling pathways. It interacts with Smad proteins and the tumor suppressor PTEN, influencing cell signaling and differentiation. WWP2 has been linked to several diseases, including Spondyloepiphyseal Dysplasia, Nishimura Type, and Cowden Syndrome 1, and its dysregulation can contribute to fibrosis, inflammation, and cancer progression. The inhibition of WWP2 has been identified as a potential therapeutic strategy for treating diseases characterized by fibrosis and inflammation, as it regulates the expression of pro-inflammatory factors and fibroblast activation. Additionally, WWP2 isoforms have distinct functions, with WWP2-N potentially suppressing TGFβ-induced epithelial-to-mesenchymal transition (EMT) and WWP2-C interacting with inhibitory Smad7.