Description: Mouse polyclonal to ADAMTS13

Description: This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants.

Description: Mouse monoclonal to ADAMTS13

Description: A polyclonal antibody against ADAMTS13. Recognizes ADAMTS13 from Human. This antibody is HRP conjugated. Tested in the following application: ELISA

Description: A polyclonal antibody against ADAMTS13. Recognizes ADAMTS13 from Human. This antibody is FITC conjugated. Tested in the following application: ELISA

Description: A polyclonal antibody against ADAMTS13. Recognizes ADAMTS13 from Human. This antibody is Biotin conjugated. Tested in the following application: ELISA

Description: For quantitative detection of human ADAMTS13 in cell culture supernates, serum and plasma(heparin, EDTA, citrate).

Description: Enzyme-linked immunosorbent assay kit for quantification of Human ADAMTS13 in samples from serum, plasma, tissue homogenates and other biological fluids.

Description: Description of target: ADAMTS13 is a zinc-containing metalloprotease enzyme. The ADAMTS13 gene is mapped to chromosome 9q34 by genomic sequence analysis. It is reported that a metal-containing proteolytic enzyme (metalloprotease) in normal plasma cleaves the peptide bond between tyrosine at position 842 and methionine at position 843 in monomeric subunits of von Willebrand factor, thereby degrading the large multimers. And it is confirmed that the ADAMTS13 gene encodes the von Willebrand factor-cleaving protease (VWFCP). ADAMTS13 is secreted in blood and degrades large vWf multimers, decreasing their activity.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: <20pg/ml

Description: Description of target: This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.127ng/mL

Description: Description of target: ;Species reactivity: Rat;Application: ;Assay info: Assay Type: Quantitative Sandwich ELISA;Sensitivity: 46.9 pg/mL