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Alexa Fluor® 488 Mouse Anti-Human CD303 Antibody (S-R662)

Alexa Fluor® 488 Mouse Anti-Human CD303 Antibody (S-R662)

Catalog Number: S0B8247 Application: FCM Reactivity: Human Conjugation: Alexa Fluor® 488 Brand: Starter
Price:
Regular price $242.00 SGD
Regular price Sale price $242.00 SGD
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Product Details

Product Specification


Host Mouse
Antigen CD303
Synonyms C-type lectin domain family 4 member C; Blood dendritic cell antigen 2 (BDCA-2); C-type lectin superfamily member 7; Dendritic lectin; BDCA2; CLECSF11; CLECSF7; DLEC; HECL; CLEC4C
Location Cell membrane
Accession Q8WTT0
Clone Number S-R662
Antibody Type Mouse mAb
Isotype IgG2a,k
Application FCM
Reactivity Hu
Positive Sample Human PBMC
Purification Protein A
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 488
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 5μl per million cells in 100μl volume Hu

Background

CD303, also known as Blood Dendritic Cell Antigen 2 (BDCA-2), is a C-type lectin receptor encoded by the CLEC4C gene, selectively expressed on human plasmacytoid dendritic cells (pDCs); it couples via the ITAM‐containing FcεRIγ adaptor to trigger Syk/Ca²⁺ signaling that drives endocytosis, the secretion of large amounts of type I interferon and pro-inflammatory cytokines, and the down-regulation of the pDC interferon response, making it both a key sentinel of viral RNA/DNA and a potential therapeutic target in autoimmunity and allergy.

Picture

FC

Flow cytometric analysis of Human CD303 expression on human PBMC (human peripheral blood mononuclear cells). Human PBMC were stained with PE/Cy7 Mouse Anti-Human CD123 Antibody and either Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Left panel) or SDT Alexa Fluor® 488 Mouse Anti-Human CD303 Antibody (Right panel) at 5μl/test. Total viable cells, as determined by Fixable Viability Dye 452 (S0D0021), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.