Human UCHL1/PGP9.5 Mouse mAb (IVD抗体) | Bioss

货号:V5803
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概述

产品编号
V5803
英文名称
Human UCHL1/PGP9.5 Mouse mAb
中文名称
神经细胞胞浆蛋白9.5/蛋白基因产物9.5单克隆抗体
英文别名
Gracile axonal dystrophy; Neuron cytoplasmic protein 9.5; Park 5; Park5; Parkinson Disease 5; PGP 9.5; PGP95; Protein gene product 9.5; Ubiquitin C terminal esterase L1; Ubiquitin C terminal hydrolase (neuron specific); Ubiquitin C terminal hydrolase; Ubiquitin carboxyl terminal esterase L1; Ubiquitin carboxyl terminal hydrolase isozyme L1; Ubiquitin carboxyl-terminal hydrolase isozyme L1; Ubiquitin thioesterase L1; Ubiquitin thiolesterase; Ubiquitin thiolesterase L1; UCH-L1; UCHL1_HUMAN.
抗体来源
Mouse
免疫原
Recombinant Human PGP9.5 Protein: 1-223/223
亚型
IgG2a
性状
Liquid
纯化方法
affinity purified by Protein A
克隆类型
Monoclonal
克隆号
4B3
理论分子量
25 kDa
储存液
0.01M PBS(pH7.4).
SWISS
Gene ID
纯度
>90% as determined by SDS-PAGE
保存条件
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍
该抗原是一种神经特异性蛋白,广泛分布于中枢与外周神经系统的神经元和神经纤维、神经内分泌细胞、肾小管段、睾丸精原细胞、Leydig细胞、卵细胞以及妊娠与非妊娠黄体内的某些细胞。用于标记神经元,对研究几种人慢性神经变性性疾病中广泛存在的细胞包涵体特征较有意义。
背景资料
catalyzes the hydrolysis of ubiquitin carboxy-terminal thiolesters to form ubiquitin and a thiol; may play a role in neuropathic pain [RGD].
Found in neuronal cell bodies and processes throughout the neocortex (at protein level). Expressed in neurons and cells of the diffuse neuroendocrine system and their tumors. Weakly expressed in ovary. Down-regulated in brains from Parkinson disease and Alzheimer disease patients.

产品应用

产品应用: ELISA

交叉反应

交叉反应: Human

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靶标

基因名
UCHL1
蛋白名
Ubiquitin carboxyl-terminal hydrolase isozyme L1
亚基
Monomer. Homodimer. Interacts with SNCA (By similarity). Interacts with COPS5.
亚细胞定位
Cytoplasm. Endoplasmic reticulum membrane. About 30% of total UCHL1 is associated with membranes in brain.
组织特异性
Found in neuronal cell bodies and processes throughout the neocortex (at protein level). Expressed in neurons and cells of the diffuse neuroendocrine system and their tumors. Weakly expressed in ovary. Down-regulated in brains from Parkinson disease and Alzheimer disease patients.
翻译后修饰
O-glycosylated.
疾病
Defects in UCHL1 are the cause of Parkinson disease type 5 (PARK5) [MIM:613643]; also known as Parkinson disease autosomal dominant 5. PARK5 is a complex neurodegenerative disorder with manifestations ranging from typical Parkinson disease to dementia with Lewy bodies. Clinical features include parkinsonian symptoms (resting tremor, rigidity, postural instability and bradykinesia), dementia, diffuse Lewy body pathology, autonomic dysfunction, hallucinations and paranoia.
相似性
Belongs to the peptidase C12 family.
功能
Ubiquitin-protein hydrolase involved both in the processing of ubiquitin precursors and of ubiquitinated proteins. This enzyme is a thiol protease that recognizes and hydrolyzes a peptide bond at the C-terminal glycine of ubiquitin. Also binds to free monoubiquitin and may prevent its degradation in lysosomes. The homodimer may have ATP-independent ubiquitin ligase activity.

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