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Mouse (Murine) MMP7 ELISA Kit for Sandwich ELISA - ABIN415611
Shukla, Kumar Shakya, Dhole, Misra: Upregulated expression of matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases in BALB/c mouse brain challenged with Japanese encephalitis virus. in Neuroimmunomodulation 2012
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Human MMP7 ELISA Kit for Sandwich ELISA - ABIN414907
Swaney, Chapman, Correa, Stebbins, Bundey, Prodanovich, Fagan, Baccei, Santini, Hutchinson, Seiders, Parr, Prasit, Evans, Lorrain: A novel, orally active LPA(1) receptor antagonist inhibits lung fibrosis in the mouse bleomycin model. in British journal of pharmacology 2010
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Mouse (Murine) MMP7 ELISA Kit for Sandwich ELISA - ABIN455846
He, Tan, Li, Wang, Nie, Hou, Liu: Matrix metalloproteinase-7 as a surrogate marker predicts renal Wnt/β-catenin activity in CKD. in Journal of the American Society of Nephrology : JASN 2012
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Human MMP7 ELISA Kit for Sandwich ELISA - ABIN625058
Garratt, Sutanto, Ling, Looi, Iosifidis, Martinovich, Shaw, Kicic-Starcevich, Knight, Ranganathan, Stick, Kicic: Matrix metalloproteinase activation by free neutrophil elastase contributes to bronchiectasis progression in early cystic fibrosis. in The European respiratory journal 2015
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Human MMP7 ELISA Kit for Sandwich ELISA - ABIN2685002
Masaki, Matsuoka, Sugiyama, Abe, Goto, Sakamoto, Atomi: Matrilysin (MMP-7) as a significant determinant of malignant potential of early invasive colorectal carcinomas. in British journal of cancer 2001
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Human MMP7 ELISA Kit for Sandwich ELISA - ABIN1672745
Kim, Lee, Choi, Yoo, Yang: Implication of MMP-9 and urokinase plasminogen activator (uPA) in the activation of pro-matrix metalloproteinase (MMP)-13. in Rheumatology international 2012
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Nishihara, Someya, Yonemoto, Ota, Itoh, Nagaoka, Takeda: Evaluation of the expression and enzyme activity of matrix metalloproteinase-7 in fetal membranes during premature rupture of membranes at term in humans. in Reproductive sciences (Thousand Oaks, Calif.) 2008
MMP7 shedding of syndecan-1 (显示 SDC1 ELISA试剂盒)/CXCL1 (显示 CXCL1 ELISA试剂盒) complexes functions as a checkpoint that restricts neutrophil activation at sites of epithelial injury.
MMP7 exerts a restrictive role on H. pylori-induced gastric injury and the development of premalignant lesions by suppressing M1 macrophage polarization.
absence of MMP7 protects mice from LPS (显示 TLR4 ELISA试剂盒)-induced intestinal permeability and lethality.
regulator of beta-catenin (显示 CTNNB1 ELISA试剂盒) function in injured lung epithelium
Angiotensin II suppresses RECK (显示 RECK ELISA试剂盒), but induces matrix metalloproteinases both in vivo and in vitro.
MMP7 regulated ciliated cell formation.
SPARC (显示 SPARC ELISA试剂盒) suppresses angiogenesis of gastric cancer by down-regulating the expression of VEGF (显示 VEGFA ELISA试剂盒) and MMP-7
Protein expression levels of MMP-7, MMP-14 (显示 MMP14 ELISA试剂盒) and ERK1/2 (显示 MAPK1/3 ELISA试剂盒) phosphorylation level were all elevated with the increasing pathological grades in brain glioma tissues.
levels of renal MMP-7 correlate with Wnt (显示 WNT2 ELISA试剂盒)/beta-catenin (显示 CTNNB1 ELISA试剂盒) activity.
STAT3 (显示 STAT3 ELISA试剂盒) plays an important role in regulation of tumor growth, invasion, and angiogenesis, which could be act by reducing MMP-7 expression in pancreatic cancer cells.
Data suggest that HAI1 (显示 SPINT1 ELISA试剂盒), a protease on the surface of colon carcinoma cells, is an MMP7 substrate; proteolysis by MMP7 releases extracellular region as soluble HAI1 (显示 SPINT1 ELISA试剂盒) (sHAI1); sHAI1 induces cancer cell aggregation; cholesterol sulfate is required for MMP-7--catalyzed generation of sHAI1. (HAI1 (显示 SPINT1 ELISA试剂盒) = hepatocyte growth factor activator inhibitor type 1 (显示 SPINT1 ELISA试剂盒); MMP7 = matrix metalloproteinase-7)
Results indicate that the matrix metallopeptidase 7 (MMP7)A-181G genotype interacts with age and gender and may serve as an early and predictive biomarker for childhood acute lymphoblastic leukemia (ALL).
The A/A genotype (OR=0.120) and A allele (OR=0.442) reduce the risk of recurrent depressive disorder occurrence in the examined polymorphisms for MMP-2 (显示 MMP2 ELISA试剂盒), MMP-7 and MMP-9 (显示 MMP9 ELISA试剂盒).
SLC12A5 (显示 SLC12A5 ELISA试剂盒) promoted the migration and invasion of BUC by enhancing MMP-7 expression.
Overexpression of LAMC2 (显示 LAMC2 ELISA试剂盒) and knockdown of CD82 (显示 CD82 ELISA试剂盒) markedly promoted GC cell invasion and activated EGFR (显示 EGFR ELISA试剂盒)/ERK1/2 (显示 MAPK1/3 ELISA试剂盒)-MMP7 signaling via upregulation of the expression of phosphorylated (p)-EGFR (显示 EGFR ELISA试剂盒), p-ERK1/2 (显示 MAPK1/3 ELISA试剂盒) and MMP7.
Matrix Metalloproteinase-7 Promoter polymorphism is associated with breast Cancer.
Data suggest that the cytoplasmic domain of Sdc2 (显示 SDC2 ELISA试剂盒) is involved in regulation of expression of MMP7 in colon carcinoma/adenocarcinoma cells; induction of MMP7 involves protein kinase C gamma (显示 PRKCG ELISA试剂盒)-mediated FAK (显示 PTK2 ELISA试剂盒)/ERK (显示 EPHB2 ELISA试剂盒) signaling. (Sdc2 (显示 SDC2 ELISA试剂盒) = syndecan-2 (显示 SDC2 ELISA试剂盒); MMP7 = matrix metalloproteinase-7; FAK (显示 PTK2 ELISA试剂盒) = focal adhesion kinase 1 (显示 PTK2 ELISA试剂盒))
We conclude that in the resected esophageal cancer an increased mRNA expression of MMP-7, MMP-10 (显示 MMP10 ELISA试剂盒) and TIMP-1 (显示 TIMP1 ELISA试剂盒) correlated with clinicopathologic features. We suggest that these genes may play a role during progression of the disease MMP-10 (显示 MMP10 ELISA试剂盒), MMP-7, TIMP-1 (显示 TIMP1 ELISA试剂盒), TIMP-2 (显示 TIMP2 ELISA试剂盒) were overexpressed in 73%, 85%, 55% and 42% of esophageal cancer samples, respectively.
plasma concentrations of MMP-7, MMP-8 (显示 MMP8 ELISA试剂盒), -9 and TIMP-1 (显示 TIMP1 ELISA试剂盒) within 96 h from the onset of acute pancreatitis symptoms are elevated in acute pancreatitis patients compared with healthy controls
ZnCo-heterobimetallic analog of cdMMP7 with Co(II) bound in the catalytic site was prepared and characterized. This study describes a well-characterized analog of MMP7 that is available for future inhibitor design efforts.
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The enzyme encoded by this gene degrades proteoglycans, fibronectin, elastin and casein and differs from most MMP family members in that it lacks a conserved C-terminal protein domain. The enzyme is involved in wound healing, and studies in mice suggest that it regulates the activity of defensins in intestinal mucosa. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3.
, matrilysin, uterine
, matrix metalloproteinase 7
, matrix metalloproteinase-7
, pump-1 protease
, uterine metalloproteinase
, Matrix metalloproteinase 7 (matrilysin)
, matrix metalloproteinase 7 (matrilysin, uterine)
, uterine matrilysin
, matrilysin-related protein