Von Willebrand Factor (VWF) Mouse Monoclonal Antibody [Clone ID: LBI2F2]

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]

Overview

Purified VWF mouse monoclonal antibody, clone LBI2F2

Synonyms

F8VWF; VWD

Gene Name

Von Willebrand factor

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

Concentration

1 mg/ml

Dilution

WB 1:2000, IHC 1:150

Form

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Buffer

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Function

Druggable Genome, Secreted Protein

Storage Conditions

Store 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.