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PerCP-Cy5.5 Rat Anti-Mouse CD335/NKP46 Antibody (S-R613)

PerCP-Cy5.5 Rat Anti-Mouse CD335/NKP46 Antibody (S-R613)

Catalog Number: S0B80558 Application: FCM Reactivity: Ms Conjugation: PerCP-Cy5.5 Brand: Starter
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Regular price $85 USD
Regular price Sale price $85 USD
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Product Details

Product Specification


Host Rat
Antigen CD335
Synonyms Natural cytotoxicity triggering receptor 1; Activating receptor 1 (mAR-1); Lymphocyte antigen 94; Natural killer cell p46-related protein (NK-p46; NKp46; mNKp46); Ly94; Ncr1
Location Cell membrane
Accession Q8C567
Clone Number S-R613
Antibody Type Rat mAb
Isotype IgG2a,k
Application FCM
Reactivity Ms
Positive Sample C57BL/6 mouse splenocytes
Purification Protein G
Concentration 0.2 mg/ml
Conjugation PerCP-Cy5.5
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.09% sodium azide

Stability & Storage

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

Dilution


application dilution species
FCM 1μg per million cells in 100μl volume Ms

Background

CD335, also known as NKp46 or Natural Cytotoxicity Triggering Receptor 1 (NCR1), is a 46 kDa type I transmembrane glycoprotein that belongs to the natural cytotoxicity receptor family. It is primarily expressed on natural killer (NK) cells and plays a crucial role in their activation and cytotoxicity. CD335 can recognize and bind to viral hemagglutinins and heparan sulfate proteoglycans on target cells, triggering NK cell-mediated cytotoxic responses. This receptor is involved in non-MHC-restricted natural cytotoxicity and is essential for the immune system's ability to detect and eliminate infected or transformed cells.

Picture

FC

Flow cytometric analysis of CD335 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Alexa Fluor® 647 Mouse Anti-Mouse NK1.1 antibody (S0B5488) and either PerCP-Cy5.5 Rat IgG2a, κ Isotype Control (left panel) or SDT PerCP-Cy5.5 Rat Anti-Mouse CD335 Antibody (right panel) at 5 μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 452 (S0B88801), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.