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抗 TRIML2 磁珠
蛋白与多肽

抗 TRIML2 磁珠

02AB00116

TRIML2, an E3 ubiquitin ligase, plays a crucial role in various cellular processes, including regulating protein degradation and modulating immune responses. Its dysfunction is linked to several diseases, notably Trichorhinophalangeal Syndrome Type II, characterized by distinct skeletal and facial abnormalities. TRIML2's ubiquitination activity is essential for maintaining cellular homeostasis, and its impairment can lead to pathological conditions, including neurodegenerative diseases. Research indicates that TRIM family proteins, including TRIML2, are involved in critical pathways such as autophagy and apoptosis, emphasizing their potential as therapeutic targets in treating diseases associated with their dysfunction. Understanding the precise mechanisms by which TRIML2 operates could provide insights into its role in disease and pave the way for novel therapeutic strategies.

Human
规格起售价
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技术参数

宿主
Mouse
靶点基因名
TRIML2
基因别名
SPRYD6
蛋白别名
tripartite motif family like 2; TRIML2
UniProt
Q8N7C3
物种
Human
应用
IP
Oligoclonal
IgG

产品详情

靶点名称
TRIML2
蛋白名称
tripartite motif family like 2
蛋白别名
Probable E3 ubiquitin-protein ligase TRIML2; RING-type E3 ubiquitin transferase TRIML2; SPRY domain-containing protein 6; Tripartite motif family-like protein 2
靶点基因名
TRIML2
基因别名
SPRYD6
UniProt
Q8N7C3
来源物种
Homo sapiens (Human)
宿主物种
Mouse
物种反应性
Human
克隆性
Oligoclonal
亚型
IgG
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
应用推荐稀释比备注
IP—50-100 μL/200 μg cell lysate

背景介绍

TRIML2, an E3 ubiquitin ligase, plays a crucial role in various cellular processes, including regulating protein degradation and modulating immune responses. Its dysfunction is linked to several diseases, notably Trichorhinophalangeal Syndrome Type II, characterized by distinct skeletal and facial abnormalities. TRIML2's ubiquitination activity is essential for maintaining cellular homeostasis, and its impairment can lead to pathological conditions, including neurodegenerative diseases. Research indicates that TRIM family proteins, including TRIML2, are involved in critical pathways such as autophagy and apoptosis, emphasizing their potential as therapeutic targets in treating diseases associated with their dysfunction. Understanding the precise mechanisms by which TRIML2 operates could provide insights into its role in disease and pave the way for novel therapeutic strategies.