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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 (14) 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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Molecular cloning and in silico analysis identify potential transcription factor binding sites in the ADAMTS3 promoter region and show that SP1 (显示 PSG1 ELISA试剂盒) downregulated ADAMTS3 transcriptional activity in osteosarcoma cell lines. As consistent with the transcriptional activity, mRNA, and protein expression levels were also decreased by SP1 (显示 PSG1 ELISA试剂盒).
Results corroborate the recent in vitro and murine data that suggest a close functional interaction between ADAMTS3 and CCBE1 (显示 CCBE1 ELISA试剂盒) in triggering VEGFR3 (显示 FLT4 ELISA试剂盒) signaling, a cornerstone for the differentiation and function of lymphatic endothelial cells.
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.
ADAMTS-3 was identified as the protease that cleaves and inactivates Reelin in the cerebral cortex and hippocampus. ADAMTS-3 was expressed in the excitatory neurons of the embryonic and postnatal cerebral cortex and hippocampus.
an ADAMTS3 knockout mouse (Adamts3(-/-)) model was created to determine in vivo the actual functions of ADAMTS3.
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