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vWF
Anti-VWF Recombinant Antibody Products
- Human Anti-VWF Recombinant Antibody (TAB-364CQ) (TAB-364CQ)
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- Species Reactivity: Human
- Type: Humanized antibody
- Application: Inhib
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- Human Anti-VWF Recombinant Antibody; Fab Fragment (TAB-364CQ-F(E)) (TAB-364CQ-F(E))
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- Species Reactivity: Human
- Type: Humanized Fab
- Application: Inhib
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- Human Anti-VWF Recombinant Antibody; scFv Fragment (TAB-364CQ-S(P)) (TAB-364CQ-S(P))
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- Species Reactivity: Human
- Type: Humanized scFv
- Application: Inhib
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- Mouse Anti-VWF Recombinant Antibody; scFv Fragment (TAB-365CQ-S(P)) (TAB-365CQ-S(P))
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- Species Reactivity: Human
- Type: Mouse scFv
- Application: Inhib
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- Human Anti-VWF Recombinant Antibody (TAB-365CQ) (TAB-365CQ)
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- Species Reactivity: Human
- Type: Chimeric antibody (mouse/human)
- Application: Inhib
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- Human Anti-VWF Recombinant Antibody; Fab Fragment (TAB-365CQ-F(E)) (TAB-365CQ-F(E))
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- Species Reactivity: Human
- Type: Chimeric antibody (mouse/human)
- Application: Inhib
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- Mouse Anti-VWF Recombinant Antibody; Fab Fragment (TAB-363CQ-F(E)) (TAB-363CQ-F(E))
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- Species Reactivity: Human
- Type: Mouse Fab
- Application: ELISA, WB, Inhib
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- Anti-Human VWF Recombinant Antibody Fab Fragment (AJvW-2) (TAB-362CQ-F(E))
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- Species Reactivity: Human
- Application: ELISA, BL
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- Anti-Human VWF Recombinant Antibody (AJvW-2) (TAB-362CQ)
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- Species Reactivity: Human
- Application: ELISA, BL
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- Mouse Anti-VWF Recombinant Antibody; scFv Fragment (TAB-363CQ-S(P)) (TAB-363CQ-S(P))
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- Species Reactivity: Human
- Type: Mouse scFv
- Application: ELISA, WB, Inhib
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- Anti-Human VWF Recombinant Antibody scFv Fragment (AJvW-2) (TAB-362CQ-S(P))
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- Species Reactivity: Human
- Application: ELISA, BL
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- Rabbit Anti-VWF Recombinant Antibody (clone AFY0080) (MOR-0109-FY)
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ICC, IHC-P, WB
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For Research Use Only. Not For Clinical Use.
This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22.
