Reactivity: | Human |
Applications: | FC |
Host Species: | Rabbit |
Isotype: | IgG |
Clonality: | Monoclonal Antibody |
Conjugation: | PE. Ex:565nm. Em:574nm. |
Gene Name: | plasminogen activator, urokinase receptor |
Gene Symbol: | PLAUR |
Synonyms: | CD87; UPAR; URKR; U-PAR |
Gene ID: | 5329 |
UniProt ID: | Q03405 |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 23-303 of human CD87/PLAUR (NP_002650.1). |
Dilution: | FC,5 μl per 10^6 cells in 100 μl volume |
Purification Method: | Affinity purification |
Concentration: | 0.02 mg/ml |
Buffer: | PBS with 0.09% Sodium azide,0.2% BSA, pH7.3. |
Storage: | Store at -20°C. Avoid freeze / thaw cycles. |
Documents: | Manual-PLAUR Antibody |
Background
This gene encodes the receptor for urokinase plasminogen activator and, given its role in localizing and promoting plasmin formation, likely influences many normal and pathological processes related to cell-surface plasminogen activation and localized degradation of the extracellular matrix. It binds both the proprotein and mature forms of urokinase plasminogen activator and permits the activation of the receptor-bound pro-enzyme by plasmin. The protein lacks transmembrane or cytoplasmic domains and may be anchored to the plasma membrane by a glycosyl-phosphatidylinositol (GPI) moiety following cleavage of the nascent polypeptide near its carboxy-terminus. However, a soluble protein is also produced in some cell types. Alternative splicing results in multiple transcript variants encoding different isoforms. The proprotein experiences several post-translational cleavage reactions that have not yet been fully defined.
Images
![]() | Flow cytometry: 1×10^6 Daudi cells (negative control,left) and U-87 MG cells (right) were surface-stained with PE Rabbit anti-Human CD87/PLAUR mAb (A26640,5 μl/Test,orange line) or PE Rabbit IgG isotype control (A24172,5 μl/Test,blue line). Non-fluorescently stained cells were used as blank control (red line). |
![]() | 1×10^6 Human PBMC were surface-stained with PE Rabbit anti-Human CD87/PLAUR mAb (A26640,5 μl/Test,orange line) or PE Rabbit IgG isotype control (A24172,5 μl/Test,blue line). Non-fluorescently stained cells were used as blank control (red line). Cells in the monocytes gate were used for analysis. |
![]() | Flow cytometry: 1×10^6 U-87 MG cells were surface-stained with PE Rabbit IgG isotype control (A24172,5 μl/Test,left) or PE Rabbit anti-Human CD87/PLAUR mAb (A26640,5 μl/Test,right). |
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