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anti-Rat (Rattus) MMP 9 Antibodies:
anti-Mouse (Murine) MMP 9 Antibodies:
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Human Polyclonal MMP 9 Primary Antibody for WB - ABIN3044382
Zhang, Chen, Qi, Wang, Xiao, Zhu: Inhibition of calcium-calmodulin-dependent kinase II suppresses cardiac fibroblast proliferation and extracellular matrix secretion. in Journal of cardiovascular pharmacology 2010
Show all 34 Pubmed References
Human Polyclonal MMP 9 Primary Antibody for ELISA, WB - ABIN3043582
Zhou, Wan, Chu, Song, Xing, Wu, Yin: Urotensin II contributes to the formation of lung adenocarcinoma inflammatory microenvironment through the NF-?B pathway in tumor-bearing nude mice. in Oncology letters 2012
Show all 34 Pubmed References
Mouse (Murine) Polyclonal MMP 9 Primary Antibody for IHC (p), ELISA - ABIN3043884
Jin, Jiang, Yang, Zhang, Yang, Zhang, Li, Yang, Ma: Acipimox attenuates atherosclerosis and enhances plaque stability in ApoE-deficient mice fed a palmitate-rich diet. in Biochemical and biophysical research communications 2012
Show all 34 Pubmed References
Human Polyclonal MMP 9 Primary Antibody for IF (p), IHC (p) - ABIN873171
Deng, Zhong, Gu, Shen, Guo: MiR-21 involve in ERK-mediated upregulation of MMP9 in the rat hippocampus following cerebral ischemia. in Brain research bulletin 2013
Show all 9 Pubmed References
Mammalian Monoclonal MMP 9 Primary Antibody for ISt, IHC - ABIN1304829
DeNiro, Al-Halafi, Al-Mohanna, Alsmadi, Al-Mohanna: Pleiotropic effects of YC-1 selectively inhibit pathological retinal neovascularization and promote physiological revascularization in a mouse model of oxygen-induced retinopathy. in Molecular pharmacology 2010
Show all 8 Pubmed References
Human Polyclonal MMP 9 Primary Antibody for IF (p), IHC (p) - ABIN668095
Zhao, Xu, He, Hua, Luo, Zuo: Expression of serum response factor in gastric carcinoma and its molecular mechanisms involved in the regulation of the invasion and migration of SGC-7901 cells. in Cancer biotherapy & radiopharmaceuticals 2013
Show all 7 Pubmed References
Human Polyclonal MMP 9 Primary Antibody for IHC (p), WB - ABIN390154
Behrens, Mathiak, Mangold, Kirdorf, Wellmann, Fogt, Rothe, Florin, Wernert: Stromal expression of invasion-promoting, matrix-degrading proteases MMP-1 and -9 and the Ets 1 transcription factor in HNPCC carcinomas and sporadic colorectal cancers. in International journal of cancer. Journal international du cancer 2003
Show all 8 Pubmed References
Human Monoclonal MMP 9 Primary Antibody for ELISA, IHC - ABIN4335100
Goktolga, Cavkaytar, Altinbas, Tapisiz, Tapisiz, Erdem: Effect of the non-specific matrix metalloproteinase inhibitor Doxycycline on endometriotic implants in an experimental rat model. in Experimental and therapeutic medicine 2015
Show all 6 Pubmed References
Cow (Bovine) Polyclonal MMP 9 Primary Antibody for IHC, WB - ABIN2777743
Nozell, Ma, Wilson, Shah, Benveniste: Class II major histocompatibility complex transactivator (CIITA) inhibits matrix metalloproteinase-9 gene expression. in The Journal of biological chemistry 2004
Show all 7 Pubmed References
Human Polyclonal MMP 9 Primary Antibody for IHC, IHC (p) - ABIN4335094
Bellini, Trentini, Manfrinato, Tamborino, Volta, Di Foggia, Fainardi, Dallocchio, Castellazzi: Matrix metalloproteinase-9 activity detected in body fluids is the result of two different enzyme forms. in Journal of biochemistry 2012
Show all 4 Pubmed References
A MMP-9-cleaved OPN fragment, OPN-32kDa, was responsible for inducing expansion of myeloid-derived suppressor cells, which may contribute to 3LL tumor's evasion of the immune response.
animals were submitted to the evaluation of Blood-Brain Barrier permeability and MMP-2 (show MMP2 Antibodies) and MMP-9 in striatum, hippocampus and cerebral cortex
p63alpha protein up-regulates heat shock protein 70 (show HSP70 Antibodies) expression via E2F1 transcription factor (show E2F1 Antibodies) 1 (show HNF1A Antibodies), promoting Wasf3/Wave3 (show WASF3 Antibodies)/MMP9 signaling and bladder cancer invasion
IL-33 (show IL33 Antibodies)-induced MMP-9 expression in the mouse monocyte/macrophage line RAW264.7.
Cleavage of beta-DG still occurred when both MMP-2 (show MMP2 Antibodies) and MMP-9 were knocked out in gamma - sarcoglycan (show SGCG Antibodies)-deficient mice. The study found that up-regulation of MMP-14 (show MMP14 Antibodies) is capable of cleaving beta-DG, and it may be involved in the pathogenesis of sarcoglycanopathy.
MMP-9's contribution to development of atherosclerotic lesions may be a direct stimulation of endothelial cells, and that PAR-1 (show MARK2 Antibodies) may serve as a receptor for MMP-9.
Results show that ablation of systemic MMP-9 initiated fatal communication between maintenance of physiological functions of MMP-9 in the bone marrow and invasive growth of pancreatic ductal adenocarcinoma via the deregulation of IL6 (show IL6 Antibodies).
MMP-9 mediates IL-17 (show IL17A Antibodies)'s capacity to inhibit myoblast differentiation during inflammatory diseases
The MURC/Cavin-4 (show MURC Antibodies) in vascular smooth muscle cells modulates abdominal aortic aneurysm (AAA (show AAAS Antibodies)) progression at the early stage via the activation of JNK (show MAPK8 Antibodies) and MMP-9. MURC/Cavin-4 (show MURC Antibodies) is a potential therapeutic target against AAA (show AAAS Antibodies) progression.
Study demonstrated evidence of beta-dystroglycan cleavage by matrix metalloproteinase-2 (show MMP2 Antibodies)/-9 in permanent middle cerebral artery occlusion mouse brains; this cleavage was implicated in aquaporin-4 (show AQP4 Antibodies) redistribution and brain edema in cerebral ischemia.
High mmp9 expression is associated with breast Cancer.
results suggest that MMP1 (show MMP1 Antibodies)-1607 1G/2G, MMP3 (show MMP3 Antibodies)-1171 5A/6A and MMP9-1562 C/T gene polymorphisms have synergistic effect on breast cancer. The interactions of MMPs clinical risk factors such as lymph node involvement has shown a strong correlation and might influence the 5-years survival rate, suggesting their potential role in the breast carcinogenesis
Ureaplasma spp (show SPEB Antibodies). carry the protease necessary for PGP (show PGPEP1 Antibodies) release, and PGP (show PGPEP1 Antibodies) and MMP-9 are increased in amniotic fluid during Ureaplasma infection, suggesting Ureaplasma spp (show SPEB Antibodies). induced collagen fragmentation contributes to preterm rupture of membranes and neutrophil influx causing chorioamnionitis.
Discovery of a highly selective chemical inhibitor of matrix metalloproteinase-9 (MMP-9) that allosterically inhibits zymogen activation
MMP-9 was shown to be useful in the diagnosis of cervical cancer, but only in the combined analysis with CA 125 (show MUC16 Antibodies), as a new diagnostic panel.
Oxidatively modified low-density lipoproteins (oxLDL) alter the function of the endoplasmic reticulum, inducing ER stress (ERS), which activates inflammatory pathways in macrophages. MMP-9 is the main protease acting on the degradation of the extracellular matrix and the ensuing destabilization of the atherosclerotic plaque. oxLDL stimulate MMP-9 expression and secretion in macrophages by mechanisms involving ERS.
The results indicated that MMP-2 (show MMP2 Antibodies) -1306C/T and MMP-9 -1562C/T polymorphisms might be associated with an increased risk of T-Cell acute lymphoblastic leukemia in a Chinese population.
Taken together, our data suggest that eupatilin inhibits TNFalpha (show TNF Antibodies)-induced MMP-2 (show MMP2 Antibodies)/-9 expression by suppressing NF-kappaB (show NFKB1 Antibodies) and MAPKAP-1 (show MAPKAP1 Antibodies) pathways via PPARalpha (show PPARA Antibodies). Our findings suggest the usefulness of eupatilin for preventing skin aging.
Levels of miR106a are modulated during cellular migration, causing a change in the levels of SIRT-1 (show SIRT1 Antibodies) mRNA by affecting its stability and the levels of SIRT-1 (show SIRT1 Antibodies) in turn can regulate the levels of MMP9.
These results suggest that the phosphorylation of STAT3 (show STAT3 Antibodies) regulates MMP-9 production in ovarian cancer, which might be responsible for its invasiveness and metastasis.
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 (show TIMP1 Antibodies), and NGAL (show LCN2 Antibodies) (also MMP2 (show MMP2 Antibodies) in 220 kDa complex) without proteolytic activity.
Data demonstrate for the first time that MMP2 (show MMP2 Antibodies) 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 (show MMP2 Antibodies), caspase-3 (show CASP3 Antibodies) and BDNF (show BDNF Antibodies)
Oxygen for newborn resuscitation increases MMP-2 (show MMP2 Antibodies)/-9 activity resulting in tissue damage and influencing remodeling processes.
contribution of MMPs to the inflammatory breakdown of the blood-CSF (show CSF2 Antibodies) barrier in vitro
The levels of matrix metalloproteinase-2 (show MMP2 Antibodies) 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 (show ALMS1 Antibodies) in vitro
Variable gene expression (eg, matrix metalloproteinase-9, CCL2 (show CCL2 Antibodies) and Lp-PLA(2 (show Lp-PLA2 Antibodies)) mRNAs), both in regard to the arterial bed and duration of disease, was associated with variable plaque development and progression.
The results showed that MMP-2 (show MMP2 Antibodies), 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.
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 (show PTH Antibodies) during metamorphosis.
MMP-9TH is responsible in the larval epithelial apoptosis through degrading ECM (show MMRN1 Antibodies) 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 (show TIMP2 Antibodies), MT1-MMP (show MMP14 Antibodies) and Gel-A, but not MT3-MMP (show MMP24 Antibodies) or TIMP-3 (show TIMP3 Antibodies), are elevated during periods of cell death and proliferation
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 (show HP Antibodies)-MMP 9 complexes appear sooner and decline more rapidly than other acute phase proteins.
Activation of cytosolic MMP-9 and MMP-2 (show MMP2 Antibodies) 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 (show TGFB1 Antibodies) and TNF-alpha (show TNF Antibodies) in IL-1beta (show IL1B Antibodies) mediated activation of proMMP-9 in pulmonary artery smooth muscle cells: involvement of an aprotinin sensitive protease.
Decreased MMP-9 and increased TIMP-1 (show TIMP1 Antibodies) 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 (show EGF Antibodies) on MMP-9 and TIMP-1 (show TIMP1 Antibodies) expression by semiquantitative RT-PCR and MMP activity by zymography.
results suggest a significant role of matrix metalloproteinase-2 (show MMP2 Antibodies) and-9 in growth and development of bovine follicle
Cells constitutively produced proMMP-9 and proMMP-2, and treatment with TNFalpha (show TNF Antibodies), hepatocyte growth factor (show HGF Antibodies), 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 (show MMP2 Antibodies), MMP-9, and TIMP-2 (show TIMP2 Antibodies) 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.
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 (show TNF Antibodies) can stimulate MMP-2 (show MMP2 Antibodies)/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 (show VEGFA Antibodies) 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 (show MMP2 Antibodies), MMP-9 and TIMP-1 (show TIMP1 Antibodies) 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 (show MMP3 Antibodies) and 9 and increase the expression of PPARgamma (show PPARG Antibodies) in atherosclerotic rabbits.
TGF-beta (show TGFB1 Antibodies) mediated MMP-9 induction may be regulated by the NF-kappaB (show NFKB1 Antibodies), Smad3 (show SMAD3 Antibodies), and JNK (show MAPK8 Antibodies) pathways, whereas the IL-1beta (show IL1B Antibodies) mediated induction may be regulated by the NF-kappaB (show NFKB1 Antibodies) and p38 (show MAPK14 Antibodies) pathways.
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 (show MMP13 Antibodies).
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 (show MMP2 Antibodies) and MMP-9 in the embryonic zebrafish.
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.
, Matrix metalloproteinase-9
, 92 kDa gelatinase
, 92 kDa type IV collagenase
, 92-kDa type IV collagenase
, gelatinase B
, matrix metalloproteinase 9 (gelatinase B 92-kDa type IV collagenase)
, matrix metalloproteinase 9 (gelatinase B, 92-kDa type IV collagenase)
, 92kD gelatinase
, 92kD type IV collagenase
, 92kDa gelatinase
, 92kDa type IV collagenase
, Gel B
, collagenase type IVB
, matrix metalloproteinase 9
, macrophage gelatinase
, matrix metalloproteinase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase)
, type V collagenase
, 75 kDa gelatinase
, type IV collagenase MMP-9
, matrix metalloproteinase 9 (gelatinase B, 92kDa matrix metalloproteinase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase)