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抗 SHPRH 磁珠
蛋白与多肽

抗 SHPRH 磁珠

02AB00061

SHPRH (SNF2 Histone Linker PHD RING Helicase) is an E3 ubiquitin ligase that plays a crucial role in DNA damage tolerance and repair mechanisms. It facilitates the transfer of ubiquitin to target proteins, particularly during genotoxic stress, which is essential for maintaining genomic stability. Dysregulation of SHPRH has been implicated in various diseases, including cancer, where its altered expression can lead to impaired DNA repair processes, contributing to tumorigenesis. Studies have shown that SHPRH interacts with other proteins involved in DNA repair, highlighting its significance in cellular responses to DNA damage. Furthermore, understanding the functional implications of SHPRH in disease contexts may provide insights into potential therapeutic targets for cancer treatment and other disorders related to genomic instability.

Human
规格起售价
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技术参数

宿主
Mouse
靶点基因名
SHPRH
基因别名
KIAA2023
蛋白别名
SNF2 histone linker PHD RING helicase; SHPRH
UniProt
Q149N8
物种
Human
应用
IP
Monoclonal
IgG1

产品详情

靶点名称
SHPRH
蛋白名称
SNF2 histone linker PHD RING helicase
蛋白别名
E3 ubiquitin-protein ligase SHPRH; RING-type E3 ubiquitin transferase SHPRH; SNF2; histone-linker; PHD and RING finger domain-containing helicase
靶点基因名
SHPRH
基因别名
KIAA2023
UniProt
Q149N8
来源物种
Homo sapiens (Human)
宿主物种
Mouse
物种反应性
Human
克隆性
Monoclonal
亚型
IgG1
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

DKTKKQAVGSPRKIQKETRKSGNKDTDSEYLPSDTSDDDDDPYYYYYKSRRNRSKLRKKLVPSTKKGKSQPFINPDSQGHCPATSDSGITDVAMSKSTCISEFNQEHETEDCAESLNHADSDVPPSNTMSPFNTSDYRFECICGELDQIDRKPRVQCLKCHLWQHAKCVN

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

背景介绍

SHPRH (SNF2 Histone Linker PHD RING Helicase) is an E3 ubiquitin ligase that plays a crucial role in DNA damage tolerance and repair mechanisms. It facilitates the transfer of ubiquitin to target proteins, particularly during genotoxic stress, which is essential for maintaining genomic stability. Dysregulation of SHPRH has been implicated in various diseases, including cancer, where its altered expression can lead to impaired DNA repair processes, contributing to tumorigenesis. Studies have shown that SHPRH interacts with other proteins involved in DNA repair, highlighting its significance in cellular responses to DNA damage. Furthermore, understanding the functional implications of SHPRH in disease contexts may provide insights into potential therapeutic targets for cancer treatment and other disorders related to genomic instability.