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ADAMTS1 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Additionally we are shipping ADAMTS1 Kits (28) and ADAMTS1 Proteins (21) and many more products for this protein.
Showing 10 out of 124 products:
Human Polyclonal ADAMTS1 Primary Antibody for IHC (p) - ABIN4278260
Pascal, Ai, Masoodi, Wang, Wang, Eisermann, Rigatti, OMalley, Ma, Wang, Dar, Parwani, Simons, Ittman, Li, Davies, Wang: Development of a reactive stroma associated with prostatic intraepithelial neoplasia in EAF2 deficient mice. in PLoS ONE 2013
Genetic haploinsufficiency of Adamts1 in mice caus (show NOS2 Antibodies)es thoracic aortic aneurysms and dissections similar to Marfan syndrome.
An ADAMTS1 blocking antibody suppressed the SPARC (show SPARC Antibodies)-induced collagen I secretion, indicating that SPARC (show SPARC Antibodies) promoted collagen production directly through ADAMTS1 interaction. In conclusion, ADAMTS1 is an important mediator of SPARC (show SPARC Antibodies)-regulated cardiac aging.
research emphasises the importance of ADAMTS5 (show ADAMTS5 Antibodies) expression in the control of influenza virus infection and highlights the potential for development of ADAMTS5 (show ADAMTS5 Antibodies)-based therapeutic strategies to reduce morbidity and mortality
increased expression of ADAMTS1 protein in macrophages and neutrophils that infiltrated aortic tissues may promote the progression of acute aortic dissection
TS5 protein functions to suppress glucose uptake in adipose-derived stromal cells and thereby inhibits the synthesis, and promotes the intracellular degradation of Acan (show ACAN Antibodies) and Vcan (show Vcan Antibodies) by an ADAMTS other than TS5.
Data suggest that ADAMTS-5 (show ADAMTS5 Antibodies) oligomerization is required for full aggrecanase (show ADAMTS4 Antibodies) activity in vitro and in situ (as seen in knee joint of mouse model of inflammatory arthritis); thus, blocking oligomerization inhibits ADAMTS-5 (show ADAMTS5 Antibodies) activity.
The resilience of casp1 (show CASP1 Antibodies)(-/-) mice to SIRS lethality is associated with a lower inflammatory response, loss of hippocampal gene coexpression patterns, and increased hippocampal Adamts1 gene expression.
Adamts-1 upregulation by inducers of pathological vascular remodeling is mediated by specific signal transduction pathways involving NFAT (show NFATC1 Antibodies) or C/EBPbeta (show CEBPB Antibodies) transcription factors.
aggrecan (show ACAN Antibodies) and brevican (show BCAN Antibodies) proteolysis is compensated in Adamts4 (show ADAMTS4 Antibodies)-/- or Adamts5 (show ADAMTS5 Antibodies)-/- mice by ADAMTS proteoglycanase (show MMP3 Antibodies) family members but a threshold of versican (show Vcan Antibodies) proteolysis is sensitive to the loss of a single ADAMTS proteoglycanase (show MMP3 Antibodies) during spinal cord injury
The present study reveals ADAMT-5 expression by mast cells(MCs (show SMCP Antibodies)) and that MC activation regulates the expression of the protease, thus implicating the ADAMT-5 of protease in MC function.
Taken together, our findings suggested that miR (show MLXIP Antibodies)-362-3p inhibits the proliferation and migration of VSMCs by directly targeting ADAMTS1, which might provide novel insight into the molecular mechanisms underlying the action of miR (show MLXIP Antibodies)-362-3p in atherosclerosis.
ADAMTS1 has diverse roles in angiogenesis, tumor microenvironment and lymphangiogenesis.
Patients with Marfan syndrome showed elevated NOS2 (show NANOS2 Antibodies) and decreased ADAMTS1 protein levels in the aorta.
Data indicate that serum versican (show Vcan Antibodies) levels were significantly decreased in polycystic ovary syndrome (PCOS) patients, and that serum ADAMTS-1 (a disintegrin and metalloproteinase with thrombospondin motif-1) and versican (show Vcan Antibodies) levels were significantly and positively correlated with each other.
Findings indicate that ADAMTS-1 has proteolytic functions in the nucleus through its interaction with aggrecan (show ACAN Antibodies) substrate in normal and tumoral breast cells.
All ADAMTS (show ADAMTS13 Antibodies) tested in our study were expressed in both stable and unstable carotid plaques, especially in smooth muscle cells and macrophages. Analysis of the expression pattern on mRNA level showed significant higher expression of ADAMTS1 in unstable plaques compared with stable plaques.
ADAMTS1 protein levels in semen were significantly lower in males with infertility. Sperm count and motility showed a negative correlation with levels of ADAMTS1 protein expression.
High ADAMTS1 expression was significantly associated with tumorigenicity of Kaposi's sarcoma-associated herpesvirus infected endothelial cells.
progesterone acts via the progesterone receptor (show PGR Antibodies) to modulate ADAMTS 1 and 4 levels in ovarian cancer cell lines.
Expression and induction of ADAMTS-1 through receptor-mediated action of progesterone in cumulus cells is one of essential requirements for gonadotropin-regulated cumulus expansion of porcine cumulus-oocyte complexes.
study indicates that disintegrin and metalloproteinase with thrombospondin motifs 1(ADAMTS1) participates in bovine endometrial remodeling
Data indicate that ADAMTS1 promoter activity and mRNA expression were increased by forskolin and human chorionic gonadotropin.
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) 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 contains two disintegrin loops and three C-terminal TS motifs and has anti-angiogenic activity. The expression of this gene may be associated with various inflammatory processes as well as development of cancer cachexia. This gene is likely to be necessary for normal growth, fertility, and organ morphology and function.
metalloproteinase with thrombospondin-like motifs-1
, ADAM metallopeptidase with thrombospondin type 1 motif, 1
, A disintegrin and metalloproteinase with thrombospondin motifs 1
, ADAM-TS 1
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 1
, A disintegrin and metalloproteinase with thrombospondin motifs 5
, ADAM-TS 5
, human metalloproteinase with thrombospondin type 1 motifs
, a disintegrin and metalloproteinase with thrombospondin motifs 1 (ADAMTS-1)
, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 1
, a disintegrin-like and metallopeptidse (reprolysin type) with thrombospondin type 1 motif, 1