The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq
Gene Description:
von Willebrand factor
Gene Alias:
F8VWF,VWD
Gene Name:
VWF
Regulation Status:
For research use only (RUO)
Detection Method:
Colorimetric
Label:
Biotin-conjugate
Sample Volume:
50 uL
Suitable Sample:
Cell Culture Samples, Plasma, Serum
Storage Instruction:
Store SP Conjugate and Biotinylated Antibody at -20°C. Store Standard at 2-8°C before reconstituting with Diluent and at -20°C after reconstituting with Diluent. Store all other components at 4°C.
Reactivity:
Human
Limit of Detection:
1.1 mU/mL
Calibration Range:
2.5 to 80 mU/mL
Product Description:
VWF (Human) ELISA Kit is a sandwich enzyme immunoassay for the quantitative measurement of human VWF.