Ubiquitin Carboxyl Terminal Hydrolase L4 (UCHL4) Antibody

Este producto es parte de UCHL - Ubiquitin C-Terminal Hydrolase L
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299€ (100 µl)

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935106861
info@markelab.com
name
Ubiquitin Carboxyl Terminal Hydrolase L4 (UCHL4) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx129331
tested applications
WB, IHC, IF/ICC

Description

Ubiquitin Carboxyl Terminal Hydrolase L4 Antibody is a Rabbit Polyclonal against Ubiquitin Carboxyl Terminal Hydrolase L4.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Ubiquitin Carboxyl Terminal Hydrolase L4 (UCHL4)
Host
Rabbit
Reactivity
Mouse
Recommended Dilution
WB: 0.01-2 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
Unconjugated
Purification
Purified by antigen-specific affinity chromatography, followed by Protein A affinity chromatography.
Size 1
100 µl
Size 2
200 µl
Size 3
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 5-7 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Alias
Ubiquitin thioesterase L4
Background
Antibody anti-UCHL4
Status
RUO

Descripción

Ubiquitin C-Terminal Hydrolase L4 (UCHL4) is a member of the deubiquitinating enzyme family, which plays a critical role in the ubiquitin-proteasome system by removing ubiquitin moieties from ubiquitinated proteins. This process regulates protein degradation, turnover, and signaling pathways. UCHL4 is specifically involved in maintaining cellular ubiquitin homeostasis, thus influencing various cellular processes, including cell cycle progression, DNA repair, and stress responses. Dysregulation of UCHL4 activity has been implicated in pathological conditions such as cancer, where it may affect the stability of key oncogenes or tumor suppressors. Additionally, UCHL4 might have a role in neurodegenerative diseases through its function in protein quality control and aggregation prevention. Understanding its precise biological mechanisms is essential for exploring its potential as a therapeutic target in diseases associated with ubiquitin pathway dysregulation.

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