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The protein encoded by ADAMTS7 is a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family. Additionally we are shipping ADAMTS7 Antibodies (55) and ADAMTS7 Proteins (9) and many more products for this protein.
Showing 6 out of 23 products:
Human ADAMTS7 ELISA Kit for Sandwich ELISA - ABIN415115
Serra, Gallelli, Butrico, Buffone, Caliò, De Caridi, Massara, Barbetta, Amato, Labonia, Mimmi, Iaccino, de Franciscis: From varices to venous ulceration: the story of chronic venous disease described by metalloproteinases. in International wound journal 2016
Show all 2 Pubmed References
Rat (Rattus) ADAMTS7 ELISA Kit for Sandwich ELISA - ABIN432446
Wu, Wang, Yu, Li, Gao, Ke, Wang, Zhou, Zheng: Association of ADAMTS-7 Levels with Cardiac Function in a Rat Model of Acute Myocardial Infarction. in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016
Therefore, these data provided the in vivo evidence, suggesting that ADAMTS-7 may play an important role in the pathogenesis of inflammatory arthritis.
Mice lacking Adamts7, Ldlr, Apoe had less lesion formation in aortas and aortic roots vs controls and less neointimal formation after femoral wire injury. Adamts7 expression was induced by injury and hyperlipidemia.
Adamts-7 deficiency substantially ameliorated neointima formation in mice at days 14 and 28 after injury. ADAMTS-7 inhibited both endothelial cell proliferation and migration.
ADAMTS-7 and TNF-alpha (show TNF ELISA Kits) form a positive feedback loop in the regulation of cartilage degradation and osteoarthritis progression.
ADAMTS7B has a domain organization with a total of eight thrombospondin type 1 repeats in its ancillary domain. Of these, seven are arranged in two distinct clusters that are separated by a mucin (show SLC13A2 ELISA Kits) domain
Findings demonstrate that ADAMTS-7, a direct target of PTHrP (show PTHLH ELISA Kits) signaling, negatively regulates endochondral bone formation by associating with and inactivating GEP (show GRN ELISA Kits) chondrogenic growth factor.
Allelic variation that associates with reduced ADAMTS7 expression confers stronger coronary heart disease protection in never-smokers than in ever-smokers.
During inflammatory conditions, AP-1 (show FOSB ELISA Kits) and Sp1 (show PSG1 ELISA Kits) sustained the expression of ADAMTS7, and ADAMTS7 sustained the expression of catabolic genes in nucleus pulposus cells
ADAMTS7 and LPA single nucleotide polymorphisms are related to a 24-h ambulatory systolic-diastolic pressure regression index.
Expression of miR (show MLXIP ELISA Kits)-26a and miR (show MLXIP ELISA Kits)-29a was significantly down regulated in leukoplakia and cancer tissues but up regulated in lichen planus tissues. Expression of target genes such as, ADAMTS7, ATP1B1 (show ATP1B1 ELISA Kits), COL4A2 (show COL4a2 ELISA Kits), CPEB3 (show CPEB3 ELISA Kits), CDK6 (show CDK6 ELISA Kits), DNMT3a (show DNMT3A ELISA Kits) and PI3KR1 was significantly down regulated in at least two of three disease types with respect to normal tissues.
Our results indicate the presence of ADAMTS-7 in human NP cells and imply its potential role in disc degeneration.
The main contribution of this study is the proposal of a pharmacophore for ADAMTS7.
The significant associations observed between this coding variant in ADAMTS7 and the risk of CAD (show CAD ELISA Kits) development.
Logistic regression analysis indicated that the association between ADAMTS-7 and heart failure after AMI (show CFD ELISA Kits) was independent from traditional cardiovascular risk factors and other biomarkers
Data conclude that ADAMTS-7 level appears to be positively associated with expression of TNF-alpha (show TNF ELISA Kits) and Phospho-NF-kappaB (show NFKB1 ELISA Kits) P65 (show GORASP1 ELISA Kits) in cartilage, which may imply its association with cartilage destruction of ONFH.
ADAMTS7 localized to cells having smooth muscle cell markers in human coronary artery disease lesions. Cultured vascular smooth muscle cells had ADAMTS7 at the cytoplasm and cell membrane, where it colocalized with markers of podosomes.
The protein encoded by this gene is a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family. Members of this 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 C-terminal TS motifs.
ADAM metallopeptidase with thrombospondin type 1 motif, 7
, A disintegrin and metalloproteinase with thrombospondin motifs 7
, ADAM-TS 7
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 7
, a disintegrin and metalloprotease with thrombospondin motifs-7 preproprotein
, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 7