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Alexa Fluor® 647 Mouse Anti-Human CD155/PVR Antibody (S-2901)

Alexa Fluor® 647 Mouse Anti-Human CD155/PVR Antibody (S-2901)

Catalog Number: S0B5687 Application: FCM Reactivity: Human Conjugation: Alexa Fluor® 647 Brand: Starter
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Regular price $220 USD
Regular price Sale price $220 USD
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Product Details

Product Specification


Host Mouse
Antigen CD155/PVR
Synonyms Poliovirus receptor; Nectin-like protein 5 (NECL-5); PVS
Location Cell membrane
Accession P15151
Clone Number S-2901
Antibody Type Mouse mAb
Isotype IgG1,k
Application FCM
Reactivity Hu
Positive Sample human peripheral blood cells
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 Hu

Background

CD155, also designated PVR (poliovirus receptor) and Necl-5, is a ~70 kDa primate-restricted type I transmembrane glycoprotein of the immunoglobulin superfamily that contains one V-type and two C2-type extracellular Ig-like domains, a 24-aa transmembrane segment and a 50-aa cytoplasmic tail; it serves as the cellular entry receptor for poliovirus, mediates cell adhesion by binding vitronectin and nectin-3, and engages immune receptors DNAM-1/CD226, CD96 and TIGIT to regulate NK-cell cytotoxicity, T-cell activation and tumor-cell recognition, while its expression—up-regulated by IFN-γ on endothelial cells and abundant on immature thymocytes, dendritic cells and epithelial/neuronal tumor cells—promotes cell migration, loss of contact inhibition and transendothelial migration.

Picture

FC

Flow cytometric analysis of CD155/PVR expression on human peripheral blood cells. Human peripheral blood cells were stained with either Alexa Fluor® 647 Mouse IgG1, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti-Human CD155/PVR Antibody (Right panel) at 1.25 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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