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anti-Human MMP 9 Antikörper:
anti-Mouse (Murine) MMP 9 Antikörper:
anti-Rat (Rattus) MMP 9 Antikörper:
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Human Polyclonal MMP 9 Primary Antibody für 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
Mouse (Murine) Polyclonal MMP 9 Primary Antibody für IHC (p), ELISA - ABIN3043884
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
Human Polyclonal MMP 9 Primary Antibody für WB - ABIN3044382
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 für 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 10 Pubmed References
Mammalian Monoclonal MMP 9 Primary Antibody für 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 für 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 für 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
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Cow (Bovine) Polyclonal MMP 9 Primary Antibody für 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 für 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
Guinea Pig Polyclonal MMP 9 Primary Antibody für 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
Our results showed that select cytokines, mitogens and inhibitors modulated A-2058 MMP-2 (zeige MMP2 Antikörper) and MMP-9 expression. They suggest the clinical potential of MMP inhibitors, especially the non-toxic ones, such as the nutrient mixture and its component EGCG in management of melanoma
results indicate a novel mechanism of alcohol craving that involves MMP-9-dependent synaptic plasticity in Central Amygdala.
The data suggest that ARTN (zeige ARTN Antikörper) and MMP-9 are involved in the occurrence, development, invasion and metastasis of EC, and play a synergistic role in the development of EC and lymphatic metastasis.
eIF4E (zeige EIF4E Antikörper) and MMP9 expression in endometrial cancer specimens suggests their potential up-regulation during carcinogenesis.
macrophage-secreted MMP-9 released HB-EGF (zeige HBEGF Antikörper) from macrophages, which increased MMP9 in OVCA433, resulting in a positive feedback loop to drive HB-EGF (zeige HBEGF Antikörper) release and increase proliferation in co-culture.
Knockdown of CREB (zeige CREB1 Antikörper) suppressed the expression of matrix metallopeptidase (zeige ECEL1 Antikörper) (MMP)2 (zeige MMP2 Antikörper)/9.
Results indicate an association between a matrix metallopeptidase 9 (MMP9) single-nucleotide polymorphisms (SNPs) at the rs2274755 locus and a decreased risk of steroid-induced osteonecrosis of the femoral head (ONFH) in a northern Chinese population.
HMOX1 (zeige HMOX1 Antikörper) negatively regulates MMP-9 expression in chronic lymphocytic leukemia cells in response to arsenic trioxide, through modulation of the p38 MAPK (zeige MAPK14 Antikörper)/AP-1 (zeige FOSB Antikörper) signaling pathway.
Study shows that expression of MMP9 expression was significantly higher in macrophages and regulated by AEG-1 (zeige MTDH Antikörper) in hypopharyngeal cancer.
Study identifies the tumor suppressor role of epithelial derived-MMP9 in colitis associated cancer via novel mechanistic pathway "MMP9-Notch1 (zeige NOTCH1 Antikörper)-ARF-p53 (zeige TP53 Antikörper) axis" regulating apoptosis, cell-cycle arrest and DNA damage.
via binding to hypoxia-responsive elements in MMP9 gene, HIF1alpha (zeige HIF1A Antikörper) stimulated MMP9 expression, and therefore appeared as a prominent intermediary in HB-EGF (zeige HBEGF Antikörper)-induced blood-brain barrier damage
Studied effects of hesperidin on skin photoaging in a hairless mouse model; results showed that hesperidin inhibited the MMP-9 related signaling pathway activated by UVB irradiation.
MMP-9 deficiency augmented AngII-induced Abdominal Aortic Aneurysms.
These results show that MMP-9/TIMP-1 (zeige TIMP1 Antikörper) 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 (zeige MLXIP Antikörper)-132 in hippocampal neurons.
M. tuberculosis infection caused enhanced MMP-1 (zeige MMP1 Antikörper), -9, and miR (zeige MLXIP Antikörper)-223 expression, with inhibited BMAL1 (zeige ARNTL Antikörper) expression. MiR (zeige MLXIP Antikörper)-223 modulated BMAL1 (zeige ARNTL Antikörper) expression via the direct binding of BMAL1 (zeige ARNTL Antikörper) 3'-UTR (zeige UTS2R Antikörper).
developed a novel selective radiolabeled MMP2 (zeige MMP2 Antikörper)/9 inhibitor, suitable for single photon emission computed tomography (SPECT) imaging that effectively targets atherosclerotic lesions in mice
MMP-2 (zeige MMP2 Antikörper) 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 (zeige YWHAZ Antikörper) 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.
Results provide evidence for the utility of MMP9 and TIMP1 (zeige TIMP1 Antikörper) 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 (zeige TIMP1 Antikörper), and NGAL (zeige LCN2 Antikörper) (also MMP2 (zeige MMP2 Antikörper) in 220 kDa complex) without proteolytic activity.
Data demonstrate for the first time that MMP2 (zeige MMP2 Antikörper) 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 (zeige MMP2 Antikörper), caspase-3 (zeige CASP3 Antikörper) and BDNF (zeige BDNF Antikörper)
Oxygen for newborn resuscitation increases MMP-2 (zeige MMP2 Antikörper)/-9 activity resulting in tissue damage and influencing remodeling processes.
contribution of MMPs to the inflammatory breakdown of the blood-CSF (zeige CSF2 Antikörper) barrier in vitro
The levels of matrix metalloproteinase-2 (zeige MMP2 Antikörper) 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 (zeige ALMS1 Antikörper) 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 (zeige HP Antikörper)-MMP 9 complexes appear sooner and decline more rapidly than other acute phase proteins.
Activation of cytosolic MMP-9 and MMP-2 (zeige MMP2 Antikörper) 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 (zeige TGFB1 Antikörper) and TNF-alpha (zeige TNF Antikörper) in IL-1beta (zeige IL1B Antikörper) mediated activation of proMMP-9 in pulmonary artery smooth muscle cells: involvement of an aprotinin sensitive protease.
Decreased MMP-9 and increased TIMP-1 (zeige TIMP1 Antikörper) 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 (zeige EGF Antikörper) on MMP-9 and TIMP-1 (zeige TIMP1 Antikörper) expression by semiquantitative RT-PCR and MMP activity by zymography.
results suggest a significant role of matrix metalloproteinase-2 (zeige MMP2 Antikörper) and-9 in growth and development of bovine follicle
Cells constitutively produced proMMP-9 and proMMP-2, and treatment with TNFalpha (zeige TNF Antikörper), hepatocyte growth factor (zeige HGF Antikörper), 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 (zeige MMP2 Antikörper), MMP-9, and TIMP-2 (zeige TIMP2 Antikörper) 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.
Mmp9 is dispensable for Hematopoietic stem cells budding, and is required for proper colonization of secondary niches.
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 (zeige MMP13 Antikörper).
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 (zeige MMP2 Antikörper) 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 (zeige PTH Antikörper) during metamorphosis.
MMP-9TH is responsible in the larval epithelial apoptosis through degrading ECM (zeige MMRN1 Antikörper) 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 (zeige TIMP2 Antikörper), MT1-MMP (zeige MMP14 Antikörper) and Gel-A, but not MT3-MMP (zeige MMP24 Antikörper) or TIMP-3 (zeige TIMP3 Antikörper), 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 (zeige TNF Antikörper) can stimulate MMP-2 (zeige MMP2 Antikörper)/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 (zeige VEGFA Antikörper) 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 (zeige MMP2 Antikörper), MMP-9 and TIMP-1 (zeige TIMP1 Antikörper) 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 (zeige MMP3 Antikörper) and 9 and increase the expression of PPARgamma (zeige PPARG Antikörper) in atherosclerotic rabbits.
TGF-beta (zeige TGFB1 Antikörper) mediated MMP-9 induction may be regulated by the NF-kappaB (zeige NFKB1 Antikörper), Smad3 (zeige SMAD3 Antikörper), and JNK (zeige MAPK8 Antikörper) pathways, whereas the IL-1beta (zeige IL1B Antikörper) mediated induction may be regulated by the NF-kappaB (zeige NFKB1 Antikörper) and p38 (zeige MAPK14 Antikörper) pathways.
The results showed that MMP-2 (zeige MMP2 Antikörper), 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