VWF anticorps (AA 1287-2770) (Fluoro488)
Aperçu rapide pour VWF anticorps (AA 1287-2770) (Fluoro488) (ABIN8053843)
Antigène
Voir toutes VWF AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1287-2770
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Fonction
- Anti-Von Willebrand Factor/VWF Antibody Fluoro488 Conjugated
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human Von Willebrand Factor/VWF recombinant protein (Position: R1287-Q2770).
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Isotype
- IgG
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Indications d'application
- Flow Cytometry, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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Date de péremption
- 12 months
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- VWF (Von Willebrand Factor (VWF))
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Autre désignation
- VWF
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Sujet
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Background: Von Willebrand factor (VWF) is a blood glycoprotein involved in hemostasis. It is mapped to 12p13.31. The VWF gene encodes von Willebrand factor (VWF), a large multimeric glycoprotein that plays a central role in the blood coagulation system, serving both as a major mediator of platelet-vessel wall interaction and platelet adhesion, and as a carrier for coagulation factor VIII. VWF released from endothelial cell Weibel-Palade bodies bound particularly avidly to the extracellular matrix. VWF deficiency or dysfunction (von Willebrand disease) leads to a bleeding tendency, which is most apparent in tissues having high blood flow shear in narrow vessels.
Gene Full Name: von Willebrand factor
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ID gène
- 7450
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UniProt
- P04275
Antigène
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