Von Willebrand Factor (VWF) Mouse Monoclonal Antibody [Clone ID: LBI2D10]
Product Specifications
Background
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]
Synonyms
F8VWF; VWD
Gene Name
Homo sapiens von Willebrand factor (VWF), mRNA.
Gene ID
7450
UniProt
P04275
Conjugation
Unconjugated
Related Pathways
Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion
Field of Research
Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion
Dilution
WB 1:2000, IHC 1:150
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome, Secreted Protein
Storage Conditions
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.
Symbol
VWF
Overview
Carrier-free (BSA/glycerol-free) VWF mouse monoclonal antibody, clone LBI2D10
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=7450
Uniprot URL
https://www.uniprot.org/uniprot/P04275
Curated Selection
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