Von Willebrand Factor (VWF) (NM_000552) Human Recombinant Protein

Specifications

Product Data
Species	Human
Expression Host	Sf9
Expression cDNA Clone or AA Sequence	Protein Sequence (showhide) A DNA sequence from TrueORF clone, RC218497, encoding the region(Met-Ala2200-Lys2813) of Homo sapiens VWF
Tag	C-DDK
Predicted MW	67 kDa
Concentration	>0.05 µg/µL as determined by microplate BCA method
Purity	> 80% as determined by SDS-PAGE and Coomassie blue staining
Buffer	50 mM Tris-HCl, 100 mM glycine, pH 8.0, 10% glycerol
Note	For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process.
Storage	Store at -80°C.
Stability	Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
Reference Data
RefSeq	NP_000543
Locus ID	7450
UniProt ID	P04275
Refseq Size	8833
Cytogenetics	12p13.31
Refseq ORF	8439
Synonyms	F8VWF; VWD
Summary	This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
Protein Families	Druggable Genome, Secreted Protein
Protein Pathways	Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion

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