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ADAMTS3 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. 再加上，我们可以发ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 3 抗体 (15) 和 ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 3 蛋白 (3)和数多这个蛋白质的别的产品。
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Findings suggest that these MMP16 (显示 MMP16 ELISA试剂盒) rs10090371, ADAMTS3 rs788935, TLL2 (显示 TLL2 ELISA试剂盒) rs10882807 and MMP9 (显示 MMP9 ELISA试剂盒) 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 (显示 ADAMTS16 ELISA试剂盒).
Data indicate that ADAMTS2 (显示 ADAMTS4 ELISA试剂盒) and 3 cleave the amino-propeptide of fibrillar collagens and regulate blood vessels homeostasis and lymphangiogenesis. [review]
ADAMTS-2 (显示 ADAMTS4 ELISA试剂盒), -3, and -13 expression, but not that of ADAMTS-14 (显示 ADAMTS14 ELISA试剂盒), are increased in plaques causing AMI (显示 CFD ELISA试剂盒) compared those associated with stable angina.
a single injection of ADAMTS5 (显示 ADAMTS5 ELISA试剂盒) siRNA induced the suppression of degradation in rabbit nucleus pulposus tissues
Studies suggest that miR (显示 MYLIP ELISA试剂盒)-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 (显示 CXCL12 ELISA试剂盒) and ADAMTS-5 (显示 ADAMTS5 ELISA试剂盒).
ADAMTS5 (显示 ADAMTS5 ELISA试剂盒) 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