| Antigen: | Factor VIII:c heavy chain |
| Clone: | RFF-VIII:c/6 |
| Subclass | IgG1 k |
| Species Raised In: | Mouse |
| Immunogen: | Purified human FVIII |
| Applications: | Immunofluorescence, Neutralising, Western |
| Growth Conditions: | RPMI + 10% FCS; non-adherent; subculture every 2-3 days; split 1:5 |
| Fusion Partner: | P3/NS/1/Ag4 |
| Relevance: | The commonest severe congenital bleeding disorder in all races is haemophilia A. The characteristic defect is a lack of coagulation factor VIII:C. Factor VIII:C is a glycoprotein that functions as a cofactor for factor IXa which, in the presence of calcium and phospholipids, converts factor X to the activated form Xa. This antibody binds to human FVIII:C heavy chain and inhibits its function. |
| References: | Goodall AH et al. 1985. Thromb Haemost. 54(4):878-91. PMID: 3937279Read more |
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