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Rabbit anti-Human von Willebrand factor (VWF) Polyclonal Antibody

The antibody against von Willebrand factor (VWF) was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 2645-2813 of human von Willebrand factor (VWF) (NP_000543.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

ADA-12641A

The antibody against von Willebrand factor (VWF) was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 2645-2813 of human von Willebrand factor (VWF) (NP_000543.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, ELISA.

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Specifications


Cat.No ADA-12641A ClonalityPolyclonal
Host SpeciesRabbitTarget Namevon Willebrand factor (VWF)
Target SynonymsVWD; F8VWF; von Willebrand factor (VWF)FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.05% proclin300, pH7.3.Purification MethodAffinity purification
Positive SamplesECV-304ApplicationELISA, WB, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 2645-2813 of human von Willebrand factor (VWF) (NP_000543.2).Target SpeciesHuman
Immunogen SequenceLPTACTIQLRGGQIMTLKRDETLQDGCDTHFCKVNERGEYFWEKRVTGCPPFDEHKCLAEGGKIMKIPGTCCDTCEEPECNDITARLQYVKVGSCKSEVEVDIHYCQGKCASKAMYSIDINDVQDQCSCCSPTRTEPMQVALHCTNGSVVYHEVLNAMECKCSPRKCSKUniprot IDP04275
Background Information
  • Uniprot Id

    P04275

  • Target Species

    Human

  • Target Name

    VWF

  • Target Full Name

    von Willebrand factor

  • Target Function

    Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet-surface receptor complex GPIb-IX-V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma.

  • Target Involvement

    von Willebrand disease 1 (VWD1); von Willebrand disease 2 (VWD2); von Willebrand disease 3 (VWD3)

  • Target Subcellular Location

    Secreted. Secreted, extracellular space, extracellular matrix. Note=Localized to storage granules.

  • Target Tissue Specificity

    Plasma.

  • Target Synonyms

    VWD; F8VWF; von Willebrand factor (VWF)

  • Target Background

    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.

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