Human 14-3-3 Sigma (SFN) Protein

Este producto es parte de SFN - stratifin
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1079€ (100 µg)

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935106861
info@markelab.com
name
Human 14-3-3 Sigma (SFN) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx693105
tested applications
SDS-PAGE

Description

Human 14-3-3 sigma Protein is a recombinant protein from Human produced in E. coli. A DNA sequence encoding the human SFN (NP_006133.1) (Met 1-Ser 248) was fused with the GST tag at the N-terminus.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
14-3-3 Sigma (SFN)
Host
E. coli
Origin
Human
Observed MW
Molecular Weight: 50.1 kDa
Sequence Fragment: Met1-Ser248
Tag: N-terminal GST tag
Validity: The validity for this protein is 12 months.
Expression
Recombinant
Purity
> 94% (SDS-PAGE)
Size 1
100 µg
Form
 
Tested Applications
SDS-PAGE
Buffer
Lyophilized from sterile 20mM Tris, 150mM NaCl, 10mM GSH, 25% glycerol, pH 8.0.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
NCBI Accession
NP_006133.1
Alias
SFN, YWHAS, Stratifin,14-3-3σ protein
Background
Protein SFN
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Stratifin (SFN) , also known as 14-3-3 sigma, is a member of the 14-3-3 protein family that acts as a critical regulator of cell cycle progression, DNA damage response, and cellular stress. It binds to phosphorylated serine/threonine residues on target proteins, facilitating their localization, stability, and activity. Stratifin is specifically involved in G2/M cell cycle checkpoint control by sequestering cyclin-dependent kinase complexes like CDC25C in the cytoplasm, preventing premature mitotic entry under DNA damage conditions. It is highly expressed in epithelial tissues and is essential for maintaining epithelial cell integrity, polarity, and stress responses. Stratifin acts as a tumor suppressor by inhibiting uncontrolled proliferation; its downregulation has been observed in breast, lung, and gastrointestinal cancers due to epigenetic silencing. Functional studies reveal its role in mediating stress-induced growth arrest and apoptosis, underscoring its importance in tumor suppression, DNA repair, and cell cycle regulation.

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