Flow cytometric analysis of human peripheral blood cells labelling human CD47 antibody at 1/200 dilution (1 μg) / (right panel) compared with a Mouse IgG1 Isotype Control / (left panel). Goat Anti- Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | CD47 |
| Synonyms | Leukocyte surface antigen CD47; Antigenic surface determinant protein OA3; Integrin-associated protein (IAP); Protein MER6; MER6 |
| Location | Cell membrane |
| Accession | Q08722 |
| Clone Number | S-3383 |
| Antibody Type | Mouse mAb |
| Isotype | IgG1 |
| Application | FCM |
| Reactivity | Hu |
| Positive Sample | Human peripheral blood cells |
| Purification | Protein G |
| 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
CD47 is a widely expressed transmembrane glycoprotein recognized for transmitting a "don't eat me" signal upon binding to signal regulatory protein alpha (SIRPα) on macrophages, thereby inhibiting phagocytosis and protecting healthy cells—especially red blood cells—from clearance. Initially identified as integrin-associated protein (IAP), it also interacts with other ligands such as thrombospondin-1 and various integrins, playing a broad role in regulating cell proliferation, migration, apoptosis, and immune homeostasis. However, many tumor cells exploit this mechanism by upregulating CD47 to evade immune surveillance, positioning CD47 as a promising target for cancer immunotherapy. Although CD47-targeting agents such as Magrolimab have shown antitumor activity in clinical trials, the widespread expression of CD47 on normal cells, particularly erythrocytes, results in significant on-target, off-tumor hematologic toxicities (e.g., anemia)—a major challenge hindering clinical translation. Current research is therefore focused on developing tumor-specific bispecific antibodies or combination strategies to mitigate this risk.
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