Flow cytometric analysis of human peripheral blood labelling human CD24 antibody at 1/2000 (0.1 μg) dilution/ (Right panel) compared with a Mouse IgG2a, κ Isotype Control / (Left panel). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody.
Product Details
Product Details
Product Specification
Host | Mouse |
Antigen | CD24 |
Synonyms | Signal transducer CD24; Small cell lung carcinoma cluster 4 antigen; CD24A |
Location | Cell membrane |
Accession | P25063 |
Clone Number | S-R576 |
Antibody Type | Mouse mAb |
Isotype | IgG2a,k |
Application | FCM |
Reactivity | Hu |
Positive Sample | human peripheral blood |
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 | 1:2000 | Hu |
Background
CD24, also known as heat stable antigen (HSA), is a mucin-type glycosylphosphatidylinositol (GPI)-anchored glycoprotein primarily expressed on the surface of hematopoietic cells such as B lymphocytes, activated T lymphocytes, monocytes, and granulocytes, as well as certain epithelial cells. It plays a critical role in cell recognition, activation, signal transduction, proliferation, differentiation, and cell extension and movement. In the context of oncology, CD24 is highly expressed in a variety of malignant tumors, including breast, ovarian, bladder, prostate, non-small cell lung, and nasopharyngeal cancers. It has immunomodulatory functions and is involved in the interaction between tumor cells and the immune system, where it can inhibit macrophage-mediated phagocytosis of tumor cells, thereby promoting immune evasion of the tumor. Its engagement with Siglec-10 on macrophages serves as a "don't eat me" signal, which is a significant mechanism of tumor immune escape. Targeting the CD24-Siglec10 axis is an area of active research in cancer immunotherapy, as it holds potential for reprogramming the tumor immune microenvironment and enhancing anti-tumor immunity.
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