Human TNF Receptor Superfamily Member 6 / CD95 / TNFRSF6 (FAS) Protein

Este producto es parte de FAS - Fas cell surface death receptor
Product Graph
234€ (5 µg)

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935106861
info@markelab.com
name
Human TNF Receptor Superfamily Member 6 / CD95 / TNFRSF6 (FAS) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx261872
tested applications
SDS-PAGE

Description

sFas Receptor Protein is a recombinant cytokine.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
TNF Receptor Superfamily Member 6 / CD95 / TNFRSF6 (FAS)
Origin
Human
Conjugation
Unconjugated
Expression
Recombinant
Purity
> 95% (SDS-PAGE and RP-HPLC)
Size 1
5 µg
Size 2
20 µg
Size 3
1 mg
Form
Lyophilized 
Tested Applications
SDS-PAGE
Availability
Shipped within 5-10 working days.
Dry Ice
No
UniProt ID
P25445
Alias
APT1,CD95,FAS1,APO-1,FASTM,ALPS1A,TNFRSF6,Apo-1 antigen,Apoptosis-mediating surface antigen FAS,FASLG receptor
Background
Protein FAS
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Tumor necrosis factor receptor superfamily member 6 (FAS), also known as CD95, is a cell surface receptor involved in the regulation of apoptosis through the extrinsic pathway FAS belongs to the TNF receptor family and triggers apoptosis upon binding with its ligand, FASL This interaction activates the caspase cascade, leading to programmed cell death FAS-mediated apoptosis plays a critical role in immune system regulation, particularly in eliminating autoreactive T-cells during immune tolerance and in regulating the survival of activated immune cells In addition to immune regulation, FAS signaling is involved in tumor progression, where altered expression of FAS or its ligand can either promote or inhibit cancer cell survival In many cancers, FAS expression is dysregulated, contributing to resistance to apoptosis and enabling tumor cell evasion from immune surveillance FAS has also been implicated in autoimmune diseases, where inappropriate activation or inhibition of FAS signaling can lead to tissue damage and chronic inflammation

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