Flow cytometric analysis of Human CD20 expression on human PBMC (human peripheral blood mononuclear cells). Human PBMC were stained with Brilliant Violet 421™ Mouse Anti-Human CD19 Antibody and either Phycoerythrin Mouse IgG2b, κ Isotype Control (Left panel) or SDT PE Mouse Anti-Human CD20 Antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
Product Details
Product Details
Product Specification
Host | Mouse |
Antigen | CD20 |
Synonyms | B-lymphocyte antigen CD20; B-lymphocyte surface antigen B1; Bp35; Leukocyte surface antigen Leu-16; Membrane-spanning 4-domains subfamily A member 1; MS4A1 |
Location | Cell membrane |
Accession | P11836 |
Clone Number | S-R449 |
Antibody Type | Mouse mAb |
Isotype | IgG2b,k |
Application | FCM |
Reactivity | Hu |
Positive Sample | human PBMC |
Purification | Protein A |
Concentration | 0.2 mg/ml |
Conjugation | PE |
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
CD20, also known as B-lymphocyte antigen CD20, is a 33–37 kDa non-glycosylated protein primarily expressed on the surface of B cells from the pre-B cell stage through maturity, but it is absent on plasma cells. It is encoded by the MS4A1 gene and belongs to the membrane-spanning 4A gene family. CD20 is a transmembrane protein with four hydrophobic transmembrane domains, one intracellular domain, and two extracellular loops. Although its exact biological function remains unclear, it is believed to play a role in B cell activation and proliferation by facilitating calcium influx. CD20 is an important therapeutic target for B cell malignancies such as chronic lymphocytic leukemia and non-Hodgkin lymphoma, as well as for some autoimmune diseases. Anti-CD20 monoclonal antibodies, like Rituximab, work through mechanisms including complement-dependent cytotoxicity, antibody-dependent cell-mediated cytotoxicity, and hyper-crosslinking.
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