Flow cytometric analysis of human CD49b expression on fresh human peripheral blood cells. Fresh human peripheral blood cells were stained with APC Mouse Anti-Human CD62p Antibody and either FITC Mouse IgG1, k Isotype Control (left panel) or SDT FITC Mouse Anti-Human CD49b Antibody (right panel) at 5 μl/test. Total viable cells, as determined by Fixable Viability Dye 452 (S0B88801), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | CD49B |
| Synonyms | Integrin alpha-2; CD49 antigen-like family member B; Collagen receptor; Platelet membrane glycoprotein Ia (GPIa); VLA-2 subunit alpha; ITGA2 |
| Location | Membrane |
| Accession | P17301 |
| Clone Number | AK-7 |
| Antibody Type | Mouse mAb |
| Isotype | IgG1,k |
| Isotype Control | S0B1529 |
| Application | FCM |
| Reactivity | Hu |
| Positive Sample | Fresh human peripheral blood cells |
| Purification | Protein G |
| Concentration | 0.2 mg/ml |
| Conjugation | FITC |
| 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
CD49b, also known as integrin alpha 2 subunit, is a 150 kDa type I transmembrane glycoprotein encoded by the ITGA2 gene. As a member of the integrin family, it must non-covalently associate with CD29 (integrin beta 1 subunit) to form the heterodimeric complex VLA-2 (Very Late Antigen-2, also known as GPIa/IIa) to exert its function. As a major receptor for laminin and collagen, the CD49b/CD29 complex plays a central role in mediating cell adhesion to the extracellular matrix. It is widely expressed on platelets, fibroblasts, endothelial cells, and various immune cell subsets, including NK cells, CD8+ T cells, and regulatory T cells. In immune responses, the expression of CD49b serves as an important functional marker: within the tumor microenvironment, infiltrating CD8+ T cells regulate their localization and migration within the collagen-rich tumor stroma through CD49b expression, and the dynamic changes in its expression (such as losing CD49b to acquire CD49a) are closely associated with T cell exhaustion. Meanwhile, a subset of effector regulatory T cells also expresses CD49b to identify their enhanced immunosuppressive function. Furthermore, as a classic surface marker for NK cells (the antigen recognized by clone DX5), CD49b is also widely used for the identification and isolation of mouse NK cells.
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