Von Willebrand factor (vWF) mediates platelet adhesion to injured endothelium, the first step in hemostasis, and helps maintain factor VIII levels. When vWF is deficient, patients have a bleeding disorder called von Willebrand disease (vWD).
| Inventor | Institute |
|---|---|
| Jacqueline Cordell | University of Oxford |
| Cat. #: | 152836 |
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| Tool sub type: | Primary antibody |
| Unit size: | 100 ug |
| Research Fields: | Stem cell biology;Tissue-specific biology |
| Application: | IHC ; WB |
| Target: | Factor VIII-related antigen (Von Willebrand factor / vWf) |
| Reactivity: | Human |
| Clone: | F8/86 |
| Host: | Mouse |
| Class: | Monoclonal |
| Product description: | Von Willebrand factor (vWF) mediates platelet adhesion to injured endothelium, the first step in hemostasis, and helps maintain factor VIII levels. When vWF is deficient, patients have a bleeding disorder called von Willebrand disease (vWD). |
|---|---|
| Conjugation: | Unconjugated |
| Isotype: | IgG1 |
| Immunogen: | Von Willebrand factor isolated from human plasma |
| Myeloma used: | P3/NS1/1-Ag4.1 |
| Target background: | Von Willebrand factor (vWF) mediates platelet adhesion to injured endothelium, the first step in hemostasis, and helps maintain factor VIII levels. When vWF is deficient, patients have a bleeding disorder called von Willebrand disease (vWD). |
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| Format: | Liquid |
|---|---|
| Concentration: | 0.9-1.1 mg/ml |
| Storage buffer: | PBS with 0.02% azide |
| Storage conditions: | -15° C to -25° C |
| Shipping conditions: | Dry ice |
| References: |
Ellis et al. 2012. J Oncol. 2012:651507. PMID: 22545050. Angiogenesis in Paget's Disease of the Vulva and the Breast: Correlation with Microvessel Density. Hussein et al. 2009. Leukemia. 23(5):852-5. PMID: 19194467. MPLW515L mutation in acute megakaryoblastic leukaemia. Disse et al. 2009. Blood. 113(4):973-80. PMID: 18945966. Phospholipase D1 is specifically required for regulated secretion of von Willebrand factor from endothelial cells. |
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