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Alexa Fluor® 647 Armenian hamster Anti-Mouse CD95 Antibody (S-R535)

Alexa Fluor® 647 Armenian hamster Anti-Mouse CD95 Antibody (S-R535)

Catalog Number: S0B8533 Application: FCM Reactivity: Mouse Conjugation: Alexa Fluor 647 Brand: Starter
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Regular price $50 USD
Regular price Sale price $50 USD
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Product Details

Product Specification


Host Armenian hamster
Antigen CD95
Synonyms Tumor necrosis factor receptor superfamily member 6; Apo-1 antigen; Apoptosis-mediating surface antigen FAS; FASLG receptor; Apt1; Tnfrsf6; Fas
Location Cell membrane
Accession P25446
Clone Number S-R535
Antibody Type Recombinant mAb
Isotype IgG
Application FCM
Reactivity Ms
Positive Sample C57BL/6 mouse thymocytes
Purification Protein G
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 647
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
FCM 1.25μl per million cells in 100μl volume Ms

Background

CD95, also known as Fas or APO-1, is a 48 kDa type-I transmembrane receptor of the TNF-receptor superfamily that, upon trimerization by its cognate ligand CD95L (FasL), assembles the death-inducing signaling complex (DISC) by recruiting the adaptor FADD and procaspase-8/10, triggering a caspase cascade that culminates in apoptosis, thereby governing immune homeostasis, peripheral tolerance, and elimination of infected or oncogenic cells, while dysregulation of this pathway contributes to autoimmune lymphoproliferative syndrome, cancer immune evasion, and resistance to chemotherapy.

Picture

FC

Flow cytometric analysis of Mouse CD95 expression on C57BL/6 mouse thymocytes. C57BL/6 mouse thymocytes were stained with either Alexa Fluor® 647 Armenian hamster IgG Isotype Control (Left panel) or SDT Alexa Fluor® 647 Armenian hamster Anti-Mouse CD95 Antibody (Right panel) at 1.25 μl/test. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.