Von Willebrand Factor (VWF) (NM_000552) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC218497L1V

  • LentiORF®

Lenti ORF particles, VWF (Myc-DDK tagged) - Human von Willebrand factor (VWF), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 21,660.00


货期*
详询

规格
    • 200 ul

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >10^7 TU/mL, 0.5 mL
    • 500 ul

CNY 2,950.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

CNY 5,230.00


Purified VWF mouse monoclonal antibody, clone OTI6C7 (formerly 6C7)
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Product Name Von Willebrand Factor (VWF) (NM_000552) Human Tagged ORF Clone Lentiviral Particle
Synonyms F8VWF; VWD
Vector pLenti-C-Myc-DDK
ACCN NM_000552
ORF Size 8439 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC218497).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_000552.3
RefSeq Size 8833 bp
RefSeq ORF 8442 bp
Locus ID 7450
Domains VWC, VWD, VWA, TIL, CT, Cys_knot
Protein Families Druggable Genome, Secreted Protein
Protein Pathways Complement and coagulation cascades, ECM-receptor interaction, Focal adhesion
MW 309.3 kDa
Gene 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]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
Customer Reviews 
Loading...