Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) Antibody (FITC)

Este producto es parte de UCHL - Ubiquitin C-Terminal Hydrolase L
Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) Antibody (FITC)
481€ (200 µl)

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Name
Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) Antibody (FITC)
Category
Primary Antibodies
Provider
Abbexa
Reference
abx274071
Tested Applications
WB, IHC, IF/ICC

Description

Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1) Antibody (FITC) is a Rabbit Polyclonal antibody conjugated to FITC against Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1).

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Ubiquitin Carboxyl Terminal Hydrolase L1 (UCHL1)
Host
Rabbit
Reactivity
Rat
Detection Method
Laser Line: 488
Excitation/Emission: 499/515
Recommended Dilution
WB: 0.5-2 µg/ml, IHC: 5-20 µg/ml, IF/ICC: 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
FITC
Isotype
IgG
Purification
Purified by antigen-specific affinity chromatography.
Size 1
200 µl
Size 2
1 ml
Form
Liquid
Tested Applications
WB, IHC, IF/ICC
Buffer
0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at 4°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Alias
HEL-117,HEL-S-53,NDGOA,PARK5 PGP 9.5,PGP9.5,PGP95,SPG79,SPG79A,UCHL-1 Uch-L1,Neuron cytoplasmic protein 9.5,Ubiquitin thioesterase L1
Background
Antibody anti-UCHL1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Background

UCHL1 is a deubiquitinating enzyme that cleaves ubiquitin from protein substrates, playing a pivotal role in the ubiquitin-proteasome system (UPS). UCHL1 is highly expressed in neurons and is crucial for maintaining protein homeostasis, axonal transport, and synaptic function. It regulates the degradation of misfolded proteins, ensuring neuronal survival and preventing neurotoxicity. Mutations in UCHL1 are linked to neurodegenerative diseases such as Parkinson’s disease and Alzheimer’s disease due to impaired protein turnover and accumulation of toxic aggregates. It also has oncogenic and tumor-suppressive roles depending on the cellular context, regulating cell cycle progression and apoptosis. Knockout studies in mice show progressive neurodegeneration, motor dysfunction, and impaired synaptic activity, highlighting UCHL1’s critical role in neuronal maintenance, proteostasis, and neuroprotection.

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