ADAMTS13, Recombinant, Human (A disintegrin and metalloproteinase with thrombospondin motifs 13 isoform 1; ADAM-TS13; von Willebrand Factor-cleaving Protease)

Catalog No : USB-A0859-61V
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Product name ADAMTS13, Recombinant, Human (A disintegrin and metalloproteinase with thrombospondin motifs 13 isoform 1; ADAM-TS13; von Willebrand Factor-cleaving Protease)
Catalog No USB-A0859-61V
Supplier’s Catalog No A0859-61V
Supplier US Biologicals
Source antigen Recombinant, CHO cells
Reactivity
Cross reactivity
Applications
Molecular weight 73
Storage -70°C
Other names
Grade Purified
Purity ≥90%, as determined by SDS-PAGE and visualized by silver stain. Endotoxin: ≤1EU/ug (LAL)
Form Supplied as a liquid in 25mM HEPES, 300mM sodium chloride, pH 8.0
Reactivity life 6 months
Note For reserch purpose only
Purity ≥90%, as determined by SDS-PAGE and visualized by silver stain. Endotoxin: ≤1EU/ug (LAL)
Description ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin motifs 13), also known as von Willebran Factor (vWF) cleaving protease, is a member of the family of secreted zinc proteases with a multi-domain structure (1-3). The protein precursors consist of a signal peptide and following domains: pro, catalytic, disintegrin-like, TS type 1 motif, cystein-rich, spacer, a second set of seven TSP1 repeats, and two CUB domins. The only known substrate of ADAMTS13 is vWF, a blood glycoprotein with two homeostatic functions (4). It is required for platelet adhesion to sites of vascular damage and acts as a carrier protein for blood-clotting factor VIII in the circulation. It exists in plasma as multimers, the largest of which effectively mediate platelet adhesion. ADAMTS13 cleaves multimeric vWF in the A2 domain at the position, Tyr 1605-Met 1606. Defect in ADAMTS13 activity is a cause of congenital thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome. Lack of ADAMTS13 activity allows unusually large vWF (UlvWF) to occur in plasma (5). These UlvWF multimers have tendency to agglutinate circulating platelets at sites with high levels of shear stress to cause TTP. Recombinant protein corresponding to Gln34-Trp688 with a C-terminal 10X-His tag from human ADAMTS13 (Accession #NP_620594), expressed in CHO cell line. The purified rhADAMTS13 starts at the N-terminus of the pro domain and ends in the spacer domain. N-Terminal Sequence Analysis: Ala75 . Molecular Mass: Predicted: 73kD Observed: 90kD (reducing conditions) Biological Activity: Measured by its ability to cleave the fluorogenic peptide substrate, FRETS-VWF73. The specific activity is >10pmol/min/ug. Storage and Stability: Aliquot to avoid repeated freezing and thawing and store at -70°C. Aliquots are stable for 6 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.