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]

Overview

Carrier-free (BSA/glycerol-free) VWF mouse monoclonal antibody, clone LBI2D10

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.