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抗 PGP9.5 磁珠
蛋白与多肽

抗 PGP9.5 磁珠

02AB00137

The UCHL1 gene provides instructions for making an enzyme called ubiquitin carboxyl-terminal esterase L1 (UCH-L1). This enzyme is found in nerve cells throughout the brain and is involved in the cell machinery that breaks down (degrades) unneeded proteins. Several functions of UCH-L1 have been proposed, including ubiquitin hydrolase activity, ubiquitin ligase activity, and stabilization of the mono-ubiquitin pool. Dysfunction of UCH-L1 has been reported in various neurodegenerative diseases. Specific mutations in the UCHL1 gene, such as I93M and E7A, have been linked to early-onset Parkinson's disease and other neurological disorders, likely due to disruption of the ubiquitin-proteasome system and accumulation of toxic protein aggregates. Overexpression of UCH-L1 has also been shown to affect Alzheimer's disease pathology by regulating amyloid-beta production. Overall, the proper function of UCH-L1 appears crucial for maintaining neuronal health and preventing the development of neurodegenerative diseases.

Human
规格起售价
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技术参数

宿主
Mouse
靶点基因名
UCHL1
蛋白别名
ubiquitin C-terminal hydrolase L1; PGP9.5
UniProt
P09936
物种
Human
应用
IP
Oligoclonal
IgG

产品详情

靶点名称
PGP9.5
蛋白名称
ubiquitin C-terminal hydrolase L1
蛋白别名
Ubiquitin carboxyl-terminal hydrolase isozyme L1; UCH-L1; Neuron cytoplasmic protein 9.5; PGP 9.5; PGP9.5; Ubiquitin thioesterase L1
靶点基因名
UCHL1
UniProt
P09936
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

The UCHL1 gene provides instructions for making an enzyme called ubiquitin carboxyl-terminal esterase L1 (UCH-L1). This enzyme is found in nerve cells throughout the brain and is involved in the cell machinery that breaks down (degrades) unneeded proteins. Several functions of UCH-L1 have been proposed, including ubiquitin hydrolase activity, ubiquitin ligase activity, and stabilization of the mono-ubiquitin pool. Dysfunction of UCH-L1 has been reported in various neurodegenerative diseases. Specific mutations in the UCHL1 gene, such as I93M and E7A, have been linked to early-onset Parkinson's disease and other neurological disorders, likely due to disruption of the ubiquitin-proteasome system and accumulation of toxic protein aggregates. Overexpression of UCH-L1 has also been shown to affect Alzheimer's disease pathology by regulating amyloid-beta production. Overall, the proper function of UCH-L1 appears crucial for maintaining neuronal health and preventing the development of neurodegenerative diseases.