Flow cytometric analysis of human GPR183 (EBI2) expression on human PBMC (human peripheral blood mononuclear cell). Human PBMC were stained with Brilliant Violet 421™ Mouse Anti-Human CD19 Antibody and either Alexa Fluor® 647 Mouse IgG2a, k Isotype Control (left panel) or SDT Alexa Fluor® 647 Mouse Anti-Human GPR183(EBI2) Antibody (right panel) at 5 μl/test. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.
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 PBMC |
| Purification | Protein A |
| Concentration | 0.2 mg/ml |
| Conjugation | Alexa Fluor® 647 |
| 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 | 5μl per million cells in 100μl volume | 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.
Picture
Picture
FC
