Von Willebrand Factor (VWF) Mouse Monoclonal Antibody [Kloon ID: LBI8G8]

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, Jul 2008]

Carrier-free (BSA/glycerol-free) VWF mouse monoclonal antibody, clone LBI8G8

F8VWF; VWD

Homo sapiens von Willebrand factor (VWF), mRNA.

7450

P04275

Unconjugated

Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion

Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion

WB 1:2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome, Secreted Protein

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

VWF

https://www.ncbi.nlm.nih.gov/gene/?term=7450

https://www.uniprot.org/uniprot/P04275