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ADAMTS3 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Additionally we are shipping ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 3 Antibodies (15) and ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 3 Kits (13) and many more products for this protein.
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Findings suggest that these MMP16 (show MMP16 Proteins) rs10090371, ADAMTS3 rs788935, TLL2 (show TLL2 Proteins) rs10882807 and MMP9 (show MMP9 Proteins) rs3918251 may be promising prognostic biomarkers for cutaneous melanoma specific survival (CMSS).
The pregnancy loss rate seems to be affected by both ADAMTS-3 and ADAMTS-16.
Data indicate that ADAMTS2 and 3 cleave the amino-propeptide of fibrillar collagens and regulate blood vessels homeostasis and lymphangiogenesis. [review]
ADAMTS-2 (show ADAMTS4 Proteins), -3, and -13 expression, but not that of ADAMTS-14, are increased in plaques causing AMI (show CFD Proteins) compared those associated with stable angina.
a single injection of ADAMTS5 (show ADAMTS5 Proteins) siRNA induced the suppression of degradation in rabbit nucleus pulposus tissues
Studies suggest that miR (show MYLIP Proteins)-140 is an important regulator of cartilage development and homeostasis in cord blood-derived mesenchymal stromal cells (eCB-MSCs) that may act, in part, through the regulation of CXCL12 (show CXCL12 Proteins) and ADAMTS-5 (show ADAMTS5 Proteins).
ADAMTS5 (show ADAMTS5 Proteins) is present in degenerative suspensory ligament desmitis as a high molecular weight complex
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) 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 protein encoded by this gene is the major procollagen II N-propeptidase. A deficiency of this protein may be responsible for dermatosparaxis, a genetic defect of connective tissues.
A disintegrin and metalloproteinase with thrombospondin motifs 3
, ADAM-TS 3
, PC II-NP
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3
, procollagen II N-proteinase
, procollagen II amino propeptide-processing enzyme
, zinc metalloendopeptidase
, ADAM metallopeptidase with thrombospondin type 1 motif, 3