Tumor Necrosis Factor Receptor Superfamily Member 6 (FAS) Antibody (APC / Cyanine 7)

Este producto es parte de FAS - Fas cell surface death receptor
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468€ (100 tests)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
Tumor Necrosis Factor Receptor Superfamily Member 6 (FAS) Antibody (APC / Cyanine 7)
category
Primary Antibodies
provider
Abbexa
reference
abx140978
tested applications
FCM

Description

Tumor Necrosis Factor Receptor Superfamily Member 6 (FAS) Antibody (APC / Cyanine 7) is a Mouse  against Tumor Necrosis Factor Receptor Superfamily Member 6 (FAS).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Tumor Necrosis Factor Receptor Superfamily Member 6 (FAS)
Host
Mouse
Reactivity
Human
Conjugation
APC / Cyanine 7
Isotype
IgG1
Clone ID
E504
Size 1
100 tests
Tested Applications
FCM
Buffer
Stabilizing PBS solution containing 15 mM sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Store in the dark at 2-8°C. Avoid exposure to light. Do not freeze.
Dry Ice
No
UniProt ID
P25445
Gene ID
355
Alias
APT1,CD95,FAS1,APO-1,FASTM,ALPS1A,TNFRSF6,Apo-1 antigen,Apoptosis-mediating surface antigen FAS,FASLG receptor
Background
Antibody anti-FAS
Status
RUO

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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