Flow cytometric analysis of Human Peripheral Blood cells labelling Human GPR183 (EBI2) antibody at 1/200 (1 μg) dilution (Right panel) compared with a Mouse IgG2a, κ Isotype Control (Left panel). Goat Anti-Mouse IgG Alexa Fluor® 647 was used as the secondary antibody. Then cells were stained with CD19 - Brilliant Violet 421™ antibody separately.
Product Details
Product Details
Product Specification
Host | Mouse |
Antigen | GPR183 (EBI2) |
Synonyms | G-protein coupled receptor 183; Epstein-Barr virus-induced G-protein coupled receptor 2 (EBI2; EBV-induced G-protein coupled receptor 2; hEBI2) |
Location | Cell membrane |
Accession | P32249 |
Clone Number | S-3016 |
Antibody Type | Mouse mAb |
Isotype | IgG2a,k |
Application | FCM |
Reactivity | Hu |
Positive Sample | Human Peripheral Blood cells |
Purification | Protein A |
Concentration | 2 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS pH7.4 |
Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
application | dilution | species |
FCM | 1:200 | Hu |
Background
GPR183 (also designated Epstein–Barr virus-induced gene 2, EBI2) is a seven-transmembrane Gαi-coupled GPCR discovered through its strong up-regulation in Epstein–Barr virus–infected Burkitt lymphoma cells; it is expressed on B cells, T cells, dendritic cells and other immune and non-immune cells, binds the oxysterol 7α,25-dihydroxycholesterol (7α,25-OHC) as its most potent endogenous ligand, and drives chemotaxis and positioning of B and T cells within secondary lymphoid organs by sensing oxysterol gradients generated by the enzymes CH25H and CYP7B1; downstream signalling involves calcium mobilisation, ERK1/2 and p38 MAPK activation, β-arrestin recruitment and SRE-mediated transcription, thereby orchestrating adaptive immune responses, while genetic or pharmacologic interference with the GPR183/7α,25-OHC axis leads to impaired antibody production, defective plasma-cell localisation and altered trafficking of innate lymphoid cells, and has implicated the receptor in autoimmune, inflammatory and viral diseases, making GPR183 and its ligand attractive therapeutic targets.
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