Recombinant full-length human UCHL1 was expressed in E. coli cells using an N-terminal His tag.
Catalog No. U522-380H
Catalog No. | Pack Size | Price (USD) | |
---|---|---|---|
U522-380H-05 | 5 ug | $226 | |
U522-380H-10 | 10 ug | $325 | |
U522-380H-BULK | BULK | Contact Us |
Overview:
UCHL1 (ubiquitin carboxyl-terminal esterase L1) is a member of the peptidase C12 family and is a thiol protease that hydrolyzes the C-terminal glycine of ubiquityl esters and amides. It is expressed in the brain and neuroendocrine system and is essential for cytoplasmic protein degradation via recycling free ubiquitin. Mutations in UCHL1 are associated with Parkinson’s Disease (PD) due to its ligase and hydrolase activity, both of which are crucial for neuronal health (1). Dysfunction of the enzyme is also associated with Alzheimer’s disease as UCHL1 was found to interact with amyloid β precursor protein and regulates the production of amyloid β protein (2).
Gene Aliases:
PGP 9.5, UCH-L1, NDGOA, PGP95, SPG79, PARK5
Genbank Number:
References:
1. Liu, Y. et al: The UCH-L1 Gene Encodes Two Opposing Enzymatic Activities that Affect α-Synuclein Degradation and Parkinson's Disease Susceptibility. Cell 111: 209-218, 2002.
2. Zhang, M. et al: Overexpression of ubiquitin carboxyl-terminal hydrolase L1 (UCHL1) delays Alzheimer's progression in vivo. Scientific Reports, 4:7298, 2014.
Specific Activity:
Sample Activity Plot. For specific information on a given lot, see related technical data sheet.
Purity:
Sample Purity Data. For specific information on a given lot, see related technical data sheet.
Storage, Stability, and Shipping:
Store product at –70oC. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Molecular Weight:
25 kDa
There are no related publications available for this product.
Cancer, Cardiovascular Disease, Cell Cycle, Cellular Stress, Invasion/Metastasis, Metabolic Disorder
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