Home / UCHL1 Knockout Cell Lines

UCHL1 Knockout Cell Lines

Gene: UCHL1

Official Full Name: ubiquitin C-terminal hydrolase L1provided by HGNC

Gene Summary: The protein encoded by this gene belongs to the peptidase C12 family. This enzyme is a thiol protease that hydrolyzes a peptide bond at the C-terminal glycine of ubiquitin. This gene is specifically expressed in the neurons and in cells of the diffuse neuroendocrine system. Mutations in this gene may be associated with Parkinson disease.[provided by RefSeq, Sep 2009]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34870 UCHL1 Knockout cell line (HeLa) Human UCHL1 1:3~1:6 Negative Online Inquiry
KO34871 UCHL1 Knockout cell line (HCT 116) Human UCHL1 1:2~1:4 Negative Online Inquiry
KO34872 UCHL1 Knockout cell line (HEK293) Human UCHL1 1:3~1:6 Negative Online Inquiry
KO34873 UCHL1 Knockout cell line (A549) Human UCHL1 1:3~1:4 Negative Online Inquiry

Background

UCHL1 Gene Knockout Cell Lines are specifically engineered cellular models that have undergone precise gene modification to inactivate the UCHL1 gene, which encodes the protein ubiquitin C-terminal hydrolase L1. This product is crucial for researchers investigating the molecular mechanisms underlying neurodegenerative diseases, as UCHL1 has been implicated in the ubiquitin-proteasome system, essential for protein degradation and cellular homeostasis.

The primary function of these knockout cell lines is to provide a platform for studying UCHL1’s role in neuronal health and disease states. By comparing the UCHL1 knockout cells to their wild-type controls, researchers can explore alterations in key cellular processes such as protein degradation, response to cellular stress, and the modulation of neuroinflammation. The absence of UCHL1 facilitates the investigation of its downstream effects, allowing for a deeper understanding of its contribution to pathologies like Alzheimer’s and Parkinson’s disease.

These knockout cell lines hold significant implications in both research and clinical settings. Their usage enables academic and pharmaceutical researchers to develop targeted therapies that can alleviate the detrimental effects associated with UCHL1 dysregulation. Moreover, they serve as valuable tools in high-throughput screening assays aiming to identify small molecules that could restore normal cellular functions.

Compared to alternative models, such as transient knockdown approaches or wild-type cells, UCHL1 gene knockout cell lines provide a stable and consistent experimental framework, minimizing variability and allowing for reproducible results. This stability is critical when delving into long-term studies and therapeutic applications.

Researchers and clinicians alike will find these cell lines indispensable for elucidating UCHL1's role in disease mechanisms, driving forward their hypotheses with confidence. With our extensive expertise in genetic engineering and commitment to providing high-quality biological products, we ensure that our UCHL1 Gene Knockout Cell Lines meet the rigorous needs of modern research and clinical applications.

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.