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anti-Human MMP 9 Antibodies:
anti-Mouse (Murine) MMP 9 Antibodies:
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Human Polyclonal MMP 9 Primary Antibody for ELISA, WB - ABIN3043582
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 WB - ABIN3044382
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 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
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
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
Guinea Pig Polyclonal MMP 9 Primary Antibody for IHC, ELISA - ABIN1582307
Piña, Boutrid, Murray, Jager, Cebulla, Schefler, Ly, Alegret, Celdran, Feuer, Jockovich: Impact of tumor-associated macrophages in LH(BETA)T(AG) mice on retinal tumor progression: relation to macrophage subtype. in Investigative ophthalmology & visual science 2010
Show all 5 Pubmed References
Results show that MMP-9 SNPs-contribution to end-organ damage could be dependent of features associated with obesity and hypertension.
Data suggest that the MMP-2 (show MMP2 Antibodies) -735 CT genotype, -735 T allele and combined genotype of MMP-2 (show MMP2 Antibodies)-735TT + MMP-9-1562CC were to have protection from developing severe HIV-associated neurocognitive disorders (HAND).
MMP-9 concentrations in both plasma and CSF (show CSF2 Antibodies), measured within 48h after subarachnoid hemorrhage, were highly predictive of the occurrence of delayed cerebral ischemia.
study results suggest an association between matrix metalloproteinase 2 (show MMP2 Antibodies), matrix metalloproteinase 9 and tissue inhibitor of metalloproteinase 2 (show TIMP2 Antibodies) single nucleotide polymorphisms with sperm parameters, but not infertility
thrombin (show F2 Antibodies) stimulates a Gq/PLC (show HSPG2 Antibodies)/PKCs/p38 MAPK (show MAPK14 Antibodies) and JNK1 (show MAPK8 Antibodies)/2 cascade, which in turn triggers NF-kappaB (show NFKB1 Antibodies) activation and ultimately induces MMP-9 expression and cell migration in SK-N-SH cells.
BRD4 (show BRD4 Antibodies) phosphorylation regulates HPV E2-mediated viral transcription and cellular MMP-9 expression
To establish the non-enzymatic functions of MMP-9 that contribute to chronic lymphocytic leukemia pathology, we generated MEC-1 cells stably expressing the catalytically inactive mutant MMP- 9MutE protein and have studied their behavior in cell migration.
After a course of electroconvulsive therapy, MMP-2 (show MMP2 Antibodies) levels were significantly increased in mood disorder patients, but MMP-9 levels were significantly decreased in both mood disorder and schizophrenia patients. In mood disorder patients, there was a significant negative correlation between depressive symptoms and serum levels of MMP-2 (show MMP2 Antibodies) and a positive correlation between depressive symptoms and MMP-9.
This study shown the Increased plasma MMP-9 levels predicted short-term fatal outcome following severe traumatic brain injury.
The expression of RECK (show RECK Antibodies) in human healthy and diseased gingiva may contribute to periodontal physiological and pathological processes; low RECK (show RECK Antibodies) expression may be associated with the enhanced MMP-2 (show MMP2 Antibodies) and MMP-9 production in inflamed gingiva.
These results show that MMP-9/TIMP-1 (show TIMP1 Antibodies) system disturbance and changes of histological structure in uteri tissue are involved in fluoride-induced reproductive dysfunctions.
Synaptic levels of MMP-9 are increased following overexpression of miR (show MLXIP Antibodies)-132 in hippocampal neurons.
M. tuberculosis infection caused enhanced MMP-1 (show MMP1 Antibodies), -9, and miR (show MLXIP Antibodies)-223 expression, with inhibited BMAL1 (show ARNTL Antibodies) expression. MiR (show MLXIP Antibodies)-223 modulated BMAL1 (show ARNTL Antibodies) expression via the direct binding of BMAL1 (show ARNTL Antibodies) 3'-UTR (show UTS2R Antibodies).
developed a novel selective radiolabeled MMP2 (show MMP2 Antibodies)/9 inhibitor, suitable for single photon emission computed tomography (SPECT) imaging that effectively targets atherosclerotic lesions in mice
MMP-2 (show MMP2 Antibodies) 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 (show YWHAZ Antibodies) 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 (show NPY Antibodies) deficient mice had significantly impaired Hematopoietic stem/progenitor cell (HSPC (show PSMA7 Antibodies)) mobilization due to increased expression of HSPC (show PSMA7 Antibodies) 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 (show MMP2 Antibodies) 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.
Results provide evidence for the utility of MMP9 and TIMP1 (show TIMP1 Antibodies) 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 (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
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.
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.
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
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 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.
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