VWF rabbit pAb

VWF rabbit pAb

• 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. [provided by RefSeq, Oct 2015]

• Description :

  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. [provided by RefSeq, Oct 2015],

• UniProt :

  P04275

• Swiss Prot :

  P04275

• Reactivity :

  Human; Rat; Mouse

• Immunogen :

  Synthesized peptide derived from part region of human protein AA range: 911-960

• Target :

  VWF

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  IHC; IF

• Concentration :

  1 mg/ml

• Dilution :

  IHC-p 1:50-300

• Buffer :

  -20°C/1 year

• Molecular Weight :

  309kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  309kD

• Fragment :

  IgG

• Subcellular Location :

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

• Gene ID (Human) :

  7450