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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 试剂盒 (13) 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 抗体) 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 抗体).
Results corroborate the recent in vitro and murine data that suggest a close functional interaction between ADAMTS3 and CCBE1 (显示 CCBE1 抗体) in triggering VEGFR3 (显示 FLT4 抗体) signaling, a cornerstone for the differentiation and function of lymphatic endothelial cells.
Findings suggest that these MMP16 (显示 MMP16 抗体) rs10090371, ADAMTS3 rs788935, TLL2 (显示 TLL2 抗体) rs10882807 and MMP9 (显示 MMP9 抗体) 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 抗体).
Data indicate that ADAMTS2 (显示 ADAMTS4 抗体) and 3 cleave the amino-propeptide of fibrillar collagens and regulate blood vessels homeostasis and lymphangiogenesis. [review]
ADAMTS-2 (显示 ADAMTS4 抗体), -3, and -13 expression, but not that of ADAMTS-14 (显示 ADAMTS14 抗体), are increased in plaques causing AMI (显示 CFD 抗体) 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