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Rabbit anti-Human VWF Polyclonal Antibody

The antibody against VWF was raised in rabbit using the Human VWF as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-51358A

The antibody against VWF was raised in rabbit using the Human VWF as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$600.00

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Specifications


Cat.No ADC-51358A ClonalityPolyclonal
Host SpeciesRabbitTarget NameVWF
FormLiquidSpecies ReactivityHuman, Mouse, Rat
IsotypeIgGStorage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azide
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman VWFTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot 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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