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ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) ELISA Kits

ADAMTS13 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Additionally we are shipping ADAMTS13 Antibodies (83) and ADAMTS13 Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
ADAMTS13 279028 Q769J6
ADAMTS13 11093 Q76LX8
ADAMTS13 362091  
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Top ADAMTS13 ELISA Kits at antibodies-online.com

Showing 10 out of 27 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.127 ng/mL 0.31-20 ng/mL 96 Tests Log in to see 9 to 11 Days
$524.21
Details
Rat 15.6 pg/mL 62.5-4000 pg/mL Typical standard curve 96 Tests Log in to see 9 to 11 Days
$910.56
Details
Mouse 19.5 pg/mL 78-5000 pg/mL   96 Tests Log in to see 11 to 13 Days
$910.56
Details
Guinea Pig 0.1 ng/mL 1.0-25 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Rabbit 0.1 ng/mL 1.0-25 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Monkey 0.1 ng/mL 1.0-25 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Dog 0.1 ng/mL 1.0-25 ng/mL   96 Tests Log in to see 11 to 13 Days
$707.14
Details
Pig
  96 Tests Log in to see 11 to 13 Days
$707.14
Details
Chicken
  96 Tests Log in to see 11 to 13 Days
$707.14
Details
Sheep
  96 Tests Log in to see 11 to 13 Days
$707.14
Details

More ELISA Kits for ADAMTS13 Interaction Partners

Mouse (Murine) ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) interaction partners

  1. Results also suggest that Toxoplasma gondii-mediated apoptosis might play a pivotal role and a different type of role in the mechanism of neurodegeneration and neuropathology in the process of toxoplasma encephalitis. Furthermore, expression of ADAMTS-13 might give an idea of the progress and is critical for diagnosis of this disease.

  2. Letter: deficiency of ADAMTS13 results in increased formation of venous thrombosis in mice.

  3. ADAMTS13 substrate specificity

  4. Data indicate that the p.D187H mutation impairs ADAMTS13 activity and secretion and may contribute to thrombotic thrombocytopenic purpura.

  5. Data show that metalloendopeptidase (show THOP1 ELISA Kits) ADAMTS13 does not directly promote development of adipose tissue.

  6. findings provide further evidence on the pathophysiological role for the ADAMTS13/VWF (show VWF ELISA Kits) axis in atherosclerosis

  7. Carboxyl terminus of ADAMTS13 directly inhibits platelet aggregation and ultra large von Willebrand factor (show VWF ELISA Kits) string formation under flow in a free-thiol-dependent manner.

  8. The results indicate that the microvascular process induced by ADAMTS13 deficiency triggers complement activation on platelets and the endothelium, which may contribute to formation of thrombotic microangiopathy.

  9. model of acute myocardial infarction in ADAMTS13 gene deleted (Adamts13 -/-) mice

  10. We hypothesize that ADAMTS13 protects brain from ischemia-reperfusion injury by regulating von Willebrand factor (show VWF ELISA Kits) -dependent inflammation as well as microvascular plugging

Human ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) interaction partners

  1. IL-8 (show IL8 ELISA Kits), TNF-alpha (show TNF ELISA Kits), tissue factor (show F3 ELISA Kits), IL-8 (show IL8 ELISA Kits)+tissue factor (show F3 ELISA Kits) and TNF-alpha (show TNF ELISA Kits)+tissue factor (show F3 ELISA Kits) decreased the levels of ADAMTS13 secreted by umbilical vein endothelial cells.

  2. Significantly lower ADAMTS-13 levels and significantly higher VWF (show VWF ELISA Kits) antigen levels were concluded to be the result of a pathological process rather than an etiological factor for Venous thromboembolism.

  3. ADAMTS13 and VWF (show VWF ELISA Kits) are co-expressed in microvascular endothelial cells.

  4. ADAMTS13-a disintegrin-like metalloproteinase with thrombospondin motif type 1 member 13-regulates a key physiological process of coagulation in the circulation by cleaving VWF (show VWF ELISA Kits) multimers into small, inactive fragments. Low levels of ADAMTS13 in the blood may play a role in cardiovascular and hematological disorders, and clarifying its role may help improve disease management.

  5. ADAMTS13 activity, d-Dimer and cystatin C (show CST3 ELISA Kits) are associated with retinopathy in type 1 diabetic patients and are promising biomarkers for the diagnosis and monitoring of diabetic retinopathy

  6. von Willebrand factor (show VWF ELISA Kits) and ADAMTS-13 are associated with the occurrence of venous thromboembolism in patients with cancer.

  7. ADAMTS13 does not appear to be associated to disease severity or the hemodynamic derangement in patients with cirrhosis.

  8. ADAMTS-13 mutations differentiate between acute thrombotic microangiopathies

  9. We found a high prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway and an apparently different penetrance of ADAMTS-13 mutations.

  10. data suggest that increased levels of VWF (show VWF ELISA Kits) and reduced levels of ADAMTS13 activity may contribute to the pathogenesis of cerebral infarction.

ADAMTS13 Antigen Profile

Antigen Summary

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene is the von Willebrand Factor (vWF)-cleaving protease, which is responsible for cleaving at the site of Tyr842-Met843 of the vWF molecule. A deficiency of this enzyme is associated with thrombotic thrombocytopenic purpura. Alternative splicing of this gene generates multiple transcript variants encoding different isoforms.

Gene names and symbols associated with ADAMTS13

  • ADAM metallopeptidase with thrombospondin type 1 motif, 13 (ADAMTS13) antibody
  • ADAM metallopeptidase with thrombospondin type 1 motif, 13 (adamts13) antibody
  • ADAM metallopeptidase with thrombospondin type 1 motif, 13 (LOC100226372) antibody
  • ADAM metallopeptidase with thrombospondin type 1 motif, 12 (ADAMTS12) antibody
  • a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13 (Adamts13) antibody
  • ADAM metallopeptidase with thrombospondin type 1 motif, 13 (Adamts13) antibody
  • ADAM-TS13 antibody
  • ADAMTS-13 antibody
  • ADAMTS12 antibody
  • ADAMTS13 antibody
  • C9orf8 antibody
  • Gm710 antibody
  • vWF-CP antibody
  • VWFCP antibody

Protein level used designations for ADAMTS13

ADAM metallopeptidase with thrombospondin type 1 motif, 13 , ADAM metallopeptidase with thrombospondin type 1 motif, 13 isoform 1 preproprotein-like , A disintegrin and metalloproteinase with thrombospondin motifs 13-like , ADAM metallopeptidase with thrombospondin type 1 motif, 12 , A disintegrin and metalloproteinase with thrombospondin motifs 12 , A disintegrin and metalloproteinase with thrombospondin motifs 13 , ADAM-TS 13 , ADAM-TS13 , ADAMTS-13 , ADAMTS13 isoform IAP-b , a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 13 , vWF-CP mRNA for von Willebrand factor-cleaving , vWF-cleaving protease , von Willebrand factor-cleaving protease , a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13

GENE ID SPECIES
100069281 Equus caballus
100320289 Danio rerio
100404947 Callithrix jacchus
100481099 Ailuropoda melanoleuca
100226372 Taeniopygia guttata
427428 Gallus gallus
461952 Pan troglodytes
479369 Canis lupus familiaris
525276 Bos taurus
701750 Macaca mulatta
100068281 Equus caballus
279028 Mus musculus
11093 Homo sapiens
100630922 Canis lupus familiaris
532272 Bos taurus
362091 Rattus norvegicus
100343027 Oryctolagus cuniculus
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