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Human MMP 9 ELISA Kit for Sandwich ELISA - ABIN411333
Turner, Nagy, Esiri, Harris, Wass: Role of matrix metalloproteinase 9 in pituitary tumor behavior. in The Journal of clinical endocrinology and metabolism 2000
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Mouse (Murine) MMP 9 ELISA Kit for Sandwich ELISA - ABIN411334
Collier, Bruns, Goldberg, Gerhard: On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes. in Genomics 1991
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Human MMP 9 ELISA Kit for Sandwich ELISA - ABIN625060
Wyrębska, Gach, Szemraj, Szewczyk, Hrabec, Koszuk, Janecki, Janecka: Comparison of anti-invasive activity of parthenolide and 3-isopropyl-2-methyl-4-methyleneisoxazolidin-5-one (MZ-6) - a new compound with α-methylene-γ-lactone motif - on two breast cancer cell lines. in Chemical biology & drug design 2011
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Human MMP 9 ELISA Kit for Sandwich ELISA - ABIN415059
Jiang, Zhang, Teng, Zhang, Zhang, Huang: Downregulation of CD9 in keratinocyte contributes to cell migration via upregulation of matrix metalloproteinase-9. in PLoS ONE 2013
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Rat (Rattus) MMP 9 ELISA Kit for Sandwich ELISA - ABIN416391
Tummers, Mountain, Mix, Kirkpatrick, Cassada, Stevens, Freeman, Goldman, Grandas: Serum levels of matrix metalloproteinase-2 as a marker of intimal hyperplasia. in The Journal of surgical research 2010
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Rat (Rattus) MMP 9 ELISA Kit for Sandwich ELISA - ABIN365564
Wang, Hsieh, Wu, Yang: Endothelin-1 enhances cell migration via matrix metalloproteinase-9 up-regulation in brain astrocytes. in Journal of neurochemistry 2010
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Johnson, Chen, Pellecchia: A high-throughput screening approach to anthrax lethal factor inhibition. in Bioorganic chemistry 2007
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Mouse (Murine) MMP 9 ELISA Kit for Sandwich ELISA - ABIN415640
Chia, Pan, Tseng, Chen, Feng, Lee, Chang, Sytwu: Experimental osteoarthritis induced by surgical realignment of the patella in BALB/c mice. in The Journal of bone and joint surgery. British volume 2010
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Lin, Hou, Shen, Juan, Ko, Wang, Chen: Quercetin inhibition of tumor invasion via suppressing PKC delta/ERK/AP-1-dependent matrix metalloproteinase-9 activation in breast carcinoma cells. in Carcinogenesis 2008
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Liau, Jazag, Whang: HMGA1 is a determinant of cellular invasiveness and in vivo metastatic potential in pancreatic adenocarcinoma. in Cancer research 2006
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The expression of RECK (显示 RECK ELISA试剂盒) in human healthy and diseased gingiva may contribute to periodontal physiological and pathological processes; low RECK (显示 RECK ELISA试剂盒) expression may be associated with the enhanced MMP-2 (显示 MMP2 ELISA试剂盒) and MMP-9 production in inflamed gingiva.
MMP-9 serum activity is a biomarker for the breast cancer risk assessment.
Intermittent hypoxia confers pro-metastatic gene expression selectively through NF-kappaB in inflammatory breast cancer cells, in particular, to tenascin-C and MPP9.
Activation of Ezh2 (显示 EZH2 ELISA试剂盒) in diabetes, via trimethylation of H3K27, facilitates recruitment of the enzymes responsible for regulation of DNA methylation (显示 HELLS ELISA试剂盒) of the MMP-9 promoter, resulting in its transcriptional activation.
Report provide evidence for an intragenic DNA methylation (显示 HELLS ELISA试剂盒) in MMP9 gene that could be involved in its transcriptional regulation in breast neoplasm.
GABRA3 (显示 GABRA3 ELISA试剂盒) induced MMP-2 (显示 MMP2 ELISA试剂盒) and MMP-9 expression through activation of the JNK (显示 MAPK8 ELISA试剂盒)/AP-1 (显示 FOSB ELISA试剂盒) signaling pathway, promoting lymphatic metastasis in lung adenocarcinoma.
the DR3 (显示 TNFRSF25 ELISA试剂盒)/TL1A (显示 TNFSF15 ELISA试剂盒) pathway directly enhances human OC formation and resorptive activity, controlling expression and activation of CCL3 (显示 CCL3 ELISA试剂盒) and MMP-9.
Matrix metalloproteinase-1 (显示 MMP1 ELISA试剂盒), -8, -9 and the risk of cardiovascular complications in patients with CHD (显示 CHDH ELISA试剂盒) before and after myocardial revascularization
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 rs3918251 may be promising prognostic biomarkers for cutaneous melanoma specific survival (CMSS).
Review/Meta-analysis: MMP-9 rs3918242 variants (T allele, TT and CT genotypes) contributed to significantly increase the risk of ischemic stroke in the Chinese population.
M. tuberculosis infection caused enhanced MMP-1 (显示 MMP1 ELISA试剂盒), -9, and miR (显示 MLXIP ELISA试剂盒)-223 expression, with inhibited BMAL1 (显示 ARNTL ELISA试剂盒) expression. MiR (显示 MLXIP ELISA试剂盒)-223 modulated BMAL1 (显示 ARNTL ELISA试剂盒) expression via the direct binding of BMAL1 (显示 ARNTL ELISA试剂盒) 3'-UTR (显示 UTS2R ELISA试剂盒).
developed a novel selective radiolabeled MMP2 (显示 MMP2 ELISA试剂盒)/9 inhibitor, suitable for single photon emission computed tomography (SPECT) imaging that effectively targets atherosclerotic lesions in mice
MMP-2 (显示 MMP2 ELISA试剂盒) and MMP-9 have roles in early stages of experimental autoimmune encephalomyelitis induction; MMP-9 from an immune cell source is required in EAE for initial infiltration of leukocytes into the central nervous system
Results show that MMP-9 modulates cholesterol metabolism, at least in part, through a novel MMP-9-plasma secreted phospholipase A2 (显示 YWHAZ ELISA试剂盒) axis that affects the hepatic transcriptional responses to dietary cholesterol. Furthermore, the data suggest that dysregulation of the MMP system can result in metabolic disorder, which could lead to atherosclerosis and coronary heart disease.
These data document a novel role for MMP-9-dependent proteolysis: the regulation of several aspects of circuit maturation to constrain excitability throughout life.
NPY (显示 NPY ELISA试剂盒) deficient mice had significantly impaired Hematopoietic stem/progenitor cell (HSPC (显示 PSMA7 ELISA试剂盒)) mobilization due to increased expression of HSPC (显示 PSMA7 ELISA试剂盒) maintenance factors by reduction of matrix metalloproteinase-9 (MMP-9) activity in bone marrow.
Optical imaging demonstrated increased MMP activity in TB lesions and MMP-9 was significantly expressed in cavitary lesions.
MMP-2 (显示 MMP2 ELISA试剂盒) and -9 expression were suppressed significantly by treatment with SB-3CT. The data demonstrated, for the first time, that SB-3CT strongly reduced corneal lymphangiogenesis and macrophage infiltration during inflammation.
Grooved surfaces showed time-dependent increase in soluble mediators involved in cell fusion, CCL2 (显示 CCL2 ELISA试剂盒) and MMP-9
A MMP-9-cleaved OPN (显示 SPP1 ELISA试剂盒) fragment, OPN (显示 SPP1 ELISA试剂盒)-32kDa (显示 TXNL1 ELISA试剂盒), was responsible for inducing expansion of myeloid-derived suppressor cells, which may contribute to 3LL tumor's evasion of the immune response.
Results provide evidence for the utility of MMP9 and TIMP1 (显示 TIMP1 ELISA试剂盒) as markers of age- and lactocrine-sensitive porcine female reproductive tract development.
Increased MMP-9 expression is associated with carotid atherosclerotic plaque.
Increased expression of MMP-9 is associated with intraplaque hemorrhage in a swine model of vulnerable carotid atherosclerosis
we demonstrated the presence of high molecular weight (HMW) complexes (130, 170, and 220 kDa) containing MMP9, TIMP1 (显示 TIMP1 ELISA试剂盒), and NGAL (显示 LCN2 ELISA试剂盒) (also MMP2 (显示 MMP2 ELISA试剂盒) in 220 kDa complex) without proteolytic activity.
Data demonstrate for the first time that MMP2 (显示 MMP2 ELISA试剂盒) and MMP9 are expressed in swine ovarian follicle both in theca and granulosa layers.
FiO2 used for resuscitation affects matrix metalloproteinases MMP-9 and MMP-2 (显示 MMP2 ELISA试剂盒), caspase-3 (显示 CASP3 ELISA试剂盒) and BDNF (显示 BDNF ELISA试剂盒)
Oxygen for newborn resuscitation increases MMP-2 (显示 MMP2 ELISA试剂盒)/-9 activity resulting in tissue damage and influencing remodeling processes.
contribution of MMPs to the inflammatory breakdown of the blood-CSF (显示 CSF2 ELISA试剂盒) barrier in vitro
The levels of matrix metalloproteinase-2 (显示 MMP2 ELISA试剂盒) and matrix metalloproteinase-9 (MMP-9)in the corpus luteum of swine during luteolysis are reported.
Our data define pericyte interactions as a main inducer of endothelial MMP secretion and propose a new role for pericyte-endothelial cell crosstalk at the BBB (显示 ALMS1 ELISA试剂盒) in vitro
In diabetic retinopathy transcription of MMP-9 is regulated by AP-1 binding at both, proximal and distal sites of its promoter, and acetylation of c-Jun and c-Fos subunits is important in its regulation.
These data demonstrate that serum neutrophil haptoglobin (显示 HP ELISA试剂盒)-MMP 9 complexes appear sooner and decline more rapidly than other acute phase proteins.
Activation of cytosolic MMP-9 and MMP-2 (显示 MMP2 ELISA试剂盒) was investigated in the retinal endothelial cells incubated in high glucose for 6-96 h, and correlated with their mitochondrial accumulation and mitochondrial damage.
Role of TGF-beta1 (显示 TGFB1 ELISA试剂盒) and TNF-alpha (显示 TNF ELISA试剂盒) in IL-1beta (显示 IL1B ELISA试剂盒) mediated activation of proMMP-9 in pulmonary artery smooth muscle cells: involvement of an aprotinin sensitive protease.
Decreased MMP-9 and increased TIMP-1 (显示 TIMP1 ELISA试剂盒) expression were found in peripheral blood cells from Mycobacterium avium subsp. paratuberculosis (Map)-infected cattle after stimulation with Map lysate and Map purified protein derivative than in control cattle.
We used a trophoblast cell line (F3) derived from bovine placentomes to examine the influence of EGF (显示 EGF ELISA试剂盒) on MMP-9 and TIMP-1 (显示 TIMP1 ELISA试剂盒) expression by semiquantitative RT-PCR and MMP activity by zymography.
results suggest a significant role of matrix metalloproteinase-2 (显示 MMP2 ELISA试剂盒) and-9 in growth and development of bovine follicle
Cells constitutively produced proMMP-9 and proMMP-2, and treatment with TNFalpha (显示 TNF ELISA试剂盒), hepatocyte growth factor (显示 HGF ELISA试剂盒), and 12-O-tetradecanoylphorbol 13-acetate resulted in significant increase in level of proMMP-9 but not in level of proMMP-2.
MMP-2 and MMP-9 production in blastocysts attached to the endometrial cells is regulated by TNF-alpha and TNF-beta
Results suggest that MMP-2 (显示 MMP2 ELISA试剂盒), MMP-9, and TIMP-2 (显示 TIMP2 ELISA试剂盒) mRNAs are expressed in bovine placentomes during the gestational and postpartum periods and that these enzymes, in conjunction with steroidogenic enzymes, mediate fetal membrane detachment after parturition.
The findings of this study suggest that Mmp-9 is a protective molecule against infection by Listeria monocytogenes by engaging in migration of zebrafish macrophages to the site of infection via a non-proteolytic role.
elevated beta-oxidation-fuelled mitochondria-derived reactive oxygen species within epidermal cells helps guide matrix metalloproteinase-driven leukocyte recruitment.
Mmp9 regulates both acute and chronic tissue damage and plays an essential role in collagen reorganization during wound repair.
MeHg impairs tail development at least partially by activation of the tissue remodeling proteases Mmp9 and Mmp13 (显示 MMP13 ELISA试剂盒).
study identified mechanism by which mycobacteria induce granulomas: ESAT-6 induced MMP9 in epithelial cells neighboring infected macrophages; MMP9 enhanced recruitment of macrophages, which contributed to nascent granuloma maturation & bacterial growth
From 24h post fertilization, mmp9 expression was detected in a population of circulating white blood cells.
expression and activity of MMP-2 (显示 MMP2 ELISA试剂盒) and MMP-9 in the embryonic zebrafish.
The MMP-9 gene was duplicated and differentiated into two genes, one was specialized in a common ancestor of X. laevis and X. tropicalis expressed in degenerating and remodeling organs in response to thyroid hormone (显示 PTH ELISA试剂盒) during metamorphosis.
MMP-9TH is responsible in the larval epithelial apoptosis through degrading ECM (显示 MMRN1 ELISA试剂盒) components in the basal lamina, whereas MMP-9 is involved in the removal of dying epithelial cells during amphibian intestinal remodeling
metamorphic tail and intestine RNA levels of TIMP-2 (显示 TIMP2 ELISA试剂盒), MT1-MMP (显示 MMP14 ELISA试剂盒) and Gel-A, but not MT3-MMP (显示 MMP24 ELISA试剂盒) or TIMP-3 (显示 TIMP3 ELISA试剂盒), are elevated during periods of cell death and proliferation
Expression of MMP-9 increased after cerebral aneurysm induction, peaking at week 3, leading to reduced smooth muscle cell number, damaged endothelial cells, and damage to the aneurysm wall elastic layer.
Inflammatory factors such as TNF-alpha (显示 TNF ELISA试剂盒) can stimulate MMP-2 (显示 MMP2 ELISA试剂盒)/9 activity in corneal epithelium cells. This may be a potential manipulating mechanism of MMP expression in the pathogenesis of corneal diseases
Therefore, it was reasonable to speculate that the increased expression of VEGF (显示 VEGFA ELISA试剂盒) and MMP-9 in residual hepatic tumor cells and tumor angiogenesis post-embolization would be responsible for the increased metastatic potentiality and invasiveness.
Performing minimally invasive surgical procedures in the early stages of intracerebral hemorrhage significantly decreases MMP-9.
Increased expression of MMP-9 in spinal cord follows cervical spondylotic myelopathy.
Hemoperfusion could obviously reduce oxidative stress and the expression levels of MMP-2 (显示 MMP2 ELISA试剂盒), MMP-9 and TIMP-1 (显示 TIMP1 ELISA试剂盒) in rabbits with acute paraquat poisoning.
In experimental syringomyelia, MMP-9 plays an important role in causing edema in the presyrinx state.
Tongxinluo can inhibit the expression of MMP-3 (显示 MMP3 ELISA试剂盒) and 9 and increase the expression of PPARgamma (显示 PPARG ELISA试剂盒) in atherosclerotic rabbits.
TGF-beta (显示 TGFB1 ELISA试剂盒) mediated MMP-9 induction may be regulated by the NF-kappaB (显示 NFKB1 ELISA试剂盒), Smad3 (显示 SMAD3 ELISA试剂盒), and JNK (显示 MAPK8 ELISA试剂盒) pathways, whereas the IL-1beta (显示 IL1B ELISA试剂盒) mediated induction may be regulated by the NF-kappaB (显示 NFKB1 ELISA试剂盒) and p38 (显示 MAPK14 ELISA试剂盒) pathways.
The results showed that MMP-2 (显示 MMP2 ELISA试剂盒), MMP-9, and StAR were significantly expressed in the granulosa and thecal cells of the ovarian atretic follicles during proestrus, and were strongly expressed in the corpus luteum during metestrus.
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 type IV and V collagens. Studies in rhesus monkeys suggest that the enzyme is involved in IL-8-induced mobilization of hematopoietic progenitor cells from bone marrow, and murine studies suggest a role in tumor-associated tissue remodeling.
92 kDa gelatinase
, 92 kDa type IV collagenase
, macrophage gelatinase
, matrix metalloproteinase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase)
, matrix metalloproteinase-9
, type V collagenase
, 92kD gelatinase
, 92kD type IV collagenase
, 92kDa gelatinase
, 92kDa type IV collagenase
, Gel B
, collagenase type IVB
, gelatinase B
, matrix metalloproteinase 9
, 92-kDa type IV collagenase
, matrix metalloproteinase 9 (gelatinase B 92-kDa type IV collagenase)
, matrix metalloproteinase 9 (gelatinase B, 92-kDa type IV collagenase)
, type IV collagenase MMP-9
, Matrix metalloproteinase-9
, matrix metalloproteinase 9 (gelatinase B, 92kDa matrix metalloproteinase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase)
, 75 kDa gelatinase