The UCHL1 Biotinylated Recombinant Rabbit Monoclonal Antibody (HDAB0216) is a cutting-edge tool for researchers studying UCHL1, a protein involved in neurodegenerative diseases and cellular homeostasis. This antibody, developed using advanced recombinant technology and biotin labeling, offers high specificity and sensitivity for detecting UCHL1 in various biological samples.UCHL1, also known as ubiquitin carboxyl-terminal hydrolase L1, plays a crucial role in maintaining protein turnover and neuronal function. Dysregulation of UCHL1 has been implicated in conditions such as Parkinson's disease, Alzheimer's disease, and cancer, making it a promising target for therapeutic interventions.
The UCHL1 antibody enables researchers to analyze UCHL1 expression and localization in different cell types and tissues, providing valuable insights into its physiological and pathological functions.With its reliable performance in techniques like Western blotting and immunohistochemistry, the UCHL1 Biotinylated Recombinant Rabbit Monoclonal Antibody (HDAB0216) is a valuable tool for scientists investigating the role of UCHL1 in neurobiology, disease pathology, and drug discovery. Its versatility and specificity make it an essential component of research projects aimed at unraveling the complex mechanisms underlying neurodegenerative disorders and cellular proteostasis.
Purified from cell culture supernatant by affinity chromatography
Formulation:
Powder
Buffer:
1XPBS
Storage:
Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing).Lyophilized antibodies are shipped at ambient temperature.
Usage:
Research use only
Background:
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]
