154 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Publications
Read Publications using NB110-82382 in the following applications:
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
Antiserum
Preservative
No Preservative
Concentration
LYOPH
Purity
Unpurified
Reconstitution Instructions
Lyophilized powder, reconstituted in distilled water.
Alternate Names for ADAMTS13 Antibody
A disintegrin and metalloproteinase with thrombospondin motifs 13
a disintegrin-like and metalloprotease (reprolysin type) with thrombospondintype 1 motif, 13
ADAM metallopeptidase with thrombospondin type 1 motif, 13
ADAMTS13
ADAM-TS13
ADAMTS-13
DKFZp434C2322
EC 3.4.24.14
EC 3.4.24.82
EC 3.4.24.87
FLJ42993
MGC118899
MGC118900
TTP
TTPADAM-TS 13
vWF-cleaving protease
vWF-CP
vWF-CPC9orf8
VWFCPvon Willebrand factor-cleaving protease
Background
Von Willebrand Factor (VWF) was previously known as Factor VIII related antigenis. VWF is synthesized exclusively by endothelial cells and megakaryocytes, and stored in the intracellular granules or constitutively secreted into plasma. This glycoprotein functions as both an antihemophilic factor carrier and a platelet vessel wall mediator in the blood coagulation system. Important in the maintenance of homeostasis, it participates in platelet vessel wall interactions by forming a noncovalent complex with coagulation factor VIII at the site of vascular injury. The Von Willebrand factor has functional binding domains to platelet glycoprotein Ib, glycoprotein IIb/IIIa, collagen and heparin. Mutations in this gene or deficiencies in this protein result in Von Willebrands disease. VWD is characterized by frequent bleeding (gingival, minor skin quantitative lacerations, menorrhagia, etc.).
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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