Rat Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L3 (UCHL3) Protein (Active)

Este producto es parte de UCHL - Ubiquitin C-Terminal Hydrolase L
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1079€ (50 µg)

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935106861
info@markelab.com
name
Rat Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L3 (UCHL3) Protein (Active)
category
Proteins and Peptides
provider
Abbexa
reference
abx693438
tested applications
SDS-PAGE

Description

Rat UCHL3 Protein is a recombinant protein from Rat produced in E. coli. A DNA sequence encoding the rat UCHL3 (Q91Y78) (Glu 2-Ala 230) was fused with a polyhistidine tag at the N-terminus.

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Product specifications

CategoryProteins and Peptides
Immunogen TargetUCHL3
HostE. coli
OriginRat
Observed MWMolecular Weight: 27.5 kDa Sequence Fragment: Glu2-Ala230 Tag: N-terminal His tag Validity: The validity for this protein is 12 months.
ExpressionRecombinant
Purity> 95% (SDS-PAGE)
Size 150 µg
Form
Tested ApplicationsSDS-PAGE
BufferLyophilized from sterile PBS, pH 7.4.
AvailabilityShipped within 5-15 working days.
StorageAliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ91Y78
AliasUCH-L3,Ubiquitin thioesterase L3
BackgroundProtein UCHL3
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

UCHL3 is a deubiquitinating enzyme involved in ubiquitin recycling and protein turnover, ensuring cellular protein quality control and homeostasis. It cleaves ubiquitin precursors and removes ubiquitin chains from target proteins, preventing their premature degradation by the proteasome. UCHL3 is ubiquitously expressed and plays roles in DNA repair, apoptosis, and embryonic development. It is particularly essential for spermatogenesis, where it regulates chromatin remodeling and germ cell differentiation. Loss of UCHL3 function is associated with impaired cellular proteostasis, genomic instability, and reproductive defects. Studies show its involvement in tumor progression, where dysregulation of UCHL3 alters protein degradation pathways, contributing to cancer cell survival. Knockout models exhibit defects in germ cell development, growth retardation, and increased sensitivity to cellular stress, underscoring its importance in ubiquitin regulation, cellular stability, and reproductive biology.

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