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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
- 亚型:
IgG
- 形态:
liquid
- 保存条件:
负20摄氏度
- 克隆性:
Polyclonal antibody
- 标记物:
Non-conjugated
- 适应物种:
Human,Mouse ,Rat
- 保质期:
6个月
- 抗原来源:
Rabbit
- 目录编号:
Q9BZJ3
- 级别:
纯化级别
- 库存:
50
- 供应商:
LSM bio
- 宿主:
E. coli - derived recombinant protein
- 应用范围:
ELISA,WB,IP
- 浓度:
≥95% as determined by SDS-PAGE
- 靶点:
ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
- 抗体英文名:
anti-UCHL1/PGP9.5 antibody,UCHL1/PGP9.5 antibody
- 抗体名:
anti-UCHL1/PGP9.5 抗体,UCHL1/PGP9.5 抗体
- 规格:
100μl
UCHL1/PGP9.5抗体| UCHL1/PGP9.5 antibody
货号 PAab09218
蛋白别名 Neuron cytoplasmic protein 9.5 antibody, PARK5 antibody, PGP 9.5 antibody, PGP9.5 antibody, Ubiquitin thioesterase L1 antibody, Uch L1 antibody, UCHL1
蛋白介绍
UCHL1(Ubiquitin carboxyl-terminal hydrolase isozyme L1) is a member of a gene family whose products hydrolyze small C-terminal adducts of ubiquitin to generate the ubiquitin monomer. Expression of UCHL1 is highly specific to neurons and to cells of the diffuse neuroendocrine system and their tumors. It is present in all neurons(PMID: 6343558). This protein is present in brain at concentrations at least 50 times greater than in other organs and is a major protein component of neuronal cytoplasm (PMID:7217993). And UCHL1 is a Parkinson's disease susceptibility gene (PMID:15048890).
产品描述
anti-UCHL1/PGP9.5 antibody is a Rabbit Polyclonal antibody againstUCHL1/PGP9.5..
建议稀释比例
WB : 1:500-1:5000;IF:N/A;IP:1:1000-1:10000
IHC
Western blot
A549 cells were subjected to SDS PAGE followed by western blot with PAab09218(UCHL1 antibody) at dilution of 1:400(本抗体仅供体外科研用途,不可用于临床诊断!) "">
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文献和实验a look from the following website just by clicking "Tyrosine Phosphorylation and Dimerization" http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WSN-43F85YV-2&_user=1111158&_coverDate=06%2F29%2F2001&_rdoc=1&_fmt=full&_orig=search
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Analysis of RB Action in DNA Damage Checkpoint Response
checkpoint response: (1) transcriptional repression of E2F-regulated genes (cyclin A reporter assay); (2) induction of cell cycle arrest (Brd-U incorporation assay); and (3) inhibition of DNA double-strand break accumulation (phosphorylated-histone H2A.X
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