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TIMP1 belongs to the TIMP gene family. Zusätzlich bieten wir Ihnen TIMP1 Kits (139) und TIMP1 Proteine (64) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 307 products:
Human Monoclonal TIMP1 Primary Antibody für CyTOF, ELISA (Capture) - ABIN4899801
Li, Hou, Shao, Tang, Li: The DSCs-expressed CD82 controls the invasiveness of trophoblast cells via integrinbeta1/MAPK/MAPK3/1 signaling pathway in human first-trimester pregnancy. in Biology of reproduction 2010
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Human Monoclonal TIMP1 Primary Antibody für CyTOF, ELISA (Capture) - ABIN4899800
Naveau, Reinald, Fournier, Durand, Lafont, Coulomb, Gogly: Gingival fibroblasts inhibit MMP-1 and MMP-3 activities in an ex-vivo artery model. in Connective tissue research 2007
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Human Polyclonal TIMP1 Primary Antibody für IHC (p), WB - ABIN3044394
Jiang, Han, Li, Yang, Liu: Carboxymethyl chitosan represses tumor angiogenesis in vitro and in vivo. in Carbohydrate polymers 2015
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Human Polyclonal TIMP1 Primary Antibody für IF (cc), IF (p) - ABIN668331
Sassoli, Nosi, Tani, Chellini, Mazzanti, Quercioli, Zecchi-Orlandini, Formigli: Defining the role of mesenchymal stromal cells on the regulation of matrix metalloproteinases in skeletal muscle cells. in Experimental cell research 2014
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Cow (Bovine) Polyclonal TIMP1 Primary Antibody für IHC, ELISA - ABIN1582210
Pitteri, Kelly-Spratt, Gurley, Kennedy, Buson, Chin, Wang, Zhang, Wong, Chodosh, Nelson, Hanash, Kemp: Tumor microenvironment-derived proteins dominate the plasma proteome response during breast cancer induction and progression. in Cancer research 2011
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Human Polyclonal TIMP1 Primary Antibody für FACS, IF - ABIN390664
Safranek, Pesta, Holubec, Kulda, Dreslerova, Vrzalova, Topolcan, Pesek, Finek, Treska: Expression of MMP-7, MMP-9, TIMP-1 and TIMP-2 mRNA in lung tissue of patients with non-small cell lung cancer (NSCLC) and benign pulmonary disease. in Anticancer research 2009
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Human Monoclonal TIMP1 Primary Antibody für ELISA, WB - ABIN2476827
Koike, Vernon, Hamner, Sadoun, Reed: MT1-MMP, but not secreted MMPs, influences the migration of human microvascular endothelial cells in 3-dimensional collagen gels. in Journal of cellular biochemistry 2002
Human Monoclonal TIMP1 Primary Antibody für ELISA - ABIN2476829
Curzi-Dascalova: [Waking and sleeping E.E.G. in normal babies before 6 months of age (author's transl)]. in Revue d'électroencéphalographie et de neurophysiologie clinique 1978
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Cow (Bovine) Polyclonal TIMP1 Primary Antibody für IHC (p), ELISA - ABIN2476830
Goldraich, Ramos, Goldraich: Urography versus DMSA scan in children with vesicoureteric reflux. in Pediatric nephrology (Berlin, Germany) 1990
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Human Monoclonal TIMP1 Primary Antibody für FACS - ABIN4896673
Domeij, Modéer, Quezada, Yucel-Lindberg: Cell expression of MMP-1 and TIMP-1 in co-cultures of human gingival fibroblasts and monocytes: the involvement of ICAM-1. in Biochemical and biophysical research communications 2005
Suggest that IL-6 (zeige IL6 Antikörper) could promote the invasiveness of breast cancer cells by inducing secretion of TIMP-1 and -2, causing a disturbance in TIMP/MMP balance.
This study indicates that in our population, the COL4A3 (zeige COL4a3 Antikörper) rs55703767 polymorphism decreased the risk of KC. However, the TIMP-1 rs6609533 polymorphism was associated with an increased risk of KC.
Low MMP-8 (zeige MMP8 Antikörper)/TIMP-1 reflects left ventricle impairment in takotsubo cardiomyopathy and high TIMP-1 may help to differentiate it from acute coronary syndrome
Data show that the mean values for TIMP1, TIMP2 (zeige TIMP2 Antikörper) and MMP2 (zeige MMP2 Antikörper) were lower in survivors, MMP9 (zeige MMP9 Antikörper) was higher in survivors.
We conclude that in the resected esophageal cancer an increased mRNA expression of MMP-7 (zeige MMP7 Antikörper), MMP-10 (zeige MMP10 Antikörper) and TIMP-1 correlated with clinicopathologic features. We suggest that these genes may play a role during progression of the diseaseMMP-10, MMP-7 (zeige MMP7 Antikörper), TIMP-1, TIMP-2 (zeige TIMP2 Antikörper) were overexpressed in 73%, 85%, 55% and 42% of esophageal cancer samples, respectively.
plasma concentrations of MMP-7 (zeige MMP7 Antikörper), MMP-8 (zeige MMP8 Antikörper), -9 and TIMP-1 within 96 h from the onset of acute pancreatitis symptoms are elevated in acute pancreatitis patients compared with healthy controls
High TIMP1 expression is associated with hepatic fibrosis.
TIMP-1 was highly expressed in TNBC patients and was associated with a poor prognosis.
Results suggest a crucial role of MMP9 (zeige MMP9 Antikörper) at the early stage of carcinogenesis in the large intestine. The increase in MMP9 (zeige MMP9 Antikörper) and TIMP1 mRNA concentration and the decrease in MMP28 (zeige MMP28 Antikörper) in the large intestinal tissue may be a confirmation of cancer.
Expression of TIMP1 is i (zeige CD63 Antikörper)ncreased in chronic pancreatitis, pancreatic intra-epithelial neoplasia, and pancreatic ductal adenocarcinoma tissues from patients. TIMP1 signaling via CD63 leads to activation of hepatic stellate cells, which create an environment in the liver that increases its susceptibility to pancreatic tumor cells.
Decreased MMP-9 (zeige MMP9 Antikörper) and increased TIMP-1 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 (zeige MMP9 Antikörper) and TIMP-1 expression by semiquantitative RT-PCR and MMP activity by zymography.
Production of TIMP-1 was augmented by IL-1alpha, TNFalpha (zeige TNF Antikörper), and hepatocyte growth factor (zeige HGF Antikörper) at level of translation and was transcriptionally increased by 12-O-tetradecanoylphorbol 13-acetate. Level of TIMP-2 (zeige TIMP2 Antikörper) mRNA was not affected by any treatments.
the different temporal expression patterns of TIMP-1 and TIMP-2 (zeige TIMP2 Antikörper) suggest that TIMP-1 may be important for luteal formation and development, while TIMP-2 (zeige TIMP2 Antikörper) may play significant roles during luteal development and maintenance
analysis of species specificity of human and bovine TIMP-1 binding to mouse TIMP-1 receptor
we demonstrated the presence of high molecular weight (HMW) complexes (130, 170, and 220 kDa) containing MMP9 (zeige MMP9 Antikörper), TIMP1, and NGAL (zeige LCN2 Antikörper) (also MMP2 (zeige MMP2 Antikörper) in 220 kDa complex) without proteolytic activity.
Hemodialysis graft placement leads to early increases in wall shear stress, VEGF-A (zeige VEGFA Antikörper), pro-MMP-9 (zeige MMP9 Antikörper), MMP-2 (zeige MMP2 Antikörper), VEGFR-1 (zeige FLT1 Antikörper), VEGFR-2 (zeige KDR Antikörper), and TIMP-1, which may contribute to the development of venous stenosis.
Results indicate that leukemia inhibitory factor (LIF (zeige LIF Antikörper)) and Oncostatin M (zeige OSM Antikörper) increase the expression of MMP-1 (zeige MMP1 Antikörper), MMP-3 (zeige MMP3 Antikörper), and TIMP-1 several fold, and that their expression is reduced to basal levels in the presence of the LIF (zeige LIF Antikörper) antagonist MH35-BD.
Hemoperfusion could obviously reduce oxidative stress and the expression levels of MMP-2 (zeige MMP2 Antikörper), MMP-9 (zeige MMP9 Antikörper) and TIMP-1 in rabbits with acute paraquat poisoning.
proteomic analysis of the mesenchymal stem cells secretome identified the TIMP-1 as a potential effector molecule responsible for the anti-angiogenic properties of MSC (zeige MSC Antikörper)
TIMP1 signaling via CD63 (zeige CD63 Antikörper) leads to activation of hepatic stellate cells, which create an environment in the liver that increases its susceptibility to pancreatic tumor cells.
This study highlights a previously undescribed integral role for TIMP1 in both vascular network maturation and adaptations to ischemia or alterations in flow.
TIMP-1 was identified as a selectively upregulated component secreted from immature astrocytes from human pluripotent stem cells.
demonstrate that TIMP-2 (zeige TIMP2 Antikörper) plays a greater protective role than TIMP-1 during the pathogenesis of atherosclerosis
Our findings reveal that elevated levels of TIMP-1 impact on neutrophil homeostasis via signaling through CD63 (zeige CD63 Antikörper).
TIMP-1 is a ligand of LRP-1 (zeige LRP1 Antikörper) and we highlight a new example of its MMP-independent, cytokine-like functions.
RAB37 (zeige RAB37 Antikörper) regulates the exocytosis of TIMP1 in a nucleotide-dependent manner to inactivate MMP9 (zeige MMP9 Antikörper) migration axis in vitro and in vivo and to suppress tumor metastasis.
PDGF-D (zeige PDGFD Antikörper) intensifies fibrogenesis by interfering with the fibrolytic activity of the TIMP-1/MMP-2 (zeige MMP2 Antikörper)/MMP (zeige MMP2 Antikörper)-9 (zeige MMP9 Antikörper) system, and PDGF-D (zeige PDGFD Antikörper) signaling is mediated through both PDGF (zeige PDGFA Antikörper)-alpha and -beta receptors.
Reduced beta(2)GP I plays a role in diabetic mice related to vascular protection, inhibiting vascular lipid deposition, and plaque formation by reducing MMPs/TIMPs expression through down-regulation of the p38MAPK (zeige MAPK14 Antikörper) signaling pathway.
This gene belongs to the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases (MMPs), a group of peptidases involved in degradation of the extracellular matrix. In addition to its inhibitory role against most of the known MMPs, the encoded protein is able to promote cell proliferation in a wide range of cell types, and may also have an anti-apoptotic function. Transcription of this gene is highly inducible in response to many cytokines and hormones. In addition, the expression from some but not all inactive X chromosomes suggests that this gene inactivation is polymorphic in human females. This gene is located within intron 6 of the synapsin I gene and is transcribed in the opposite direction.
tissue inhibitor of matrix metalloproteinase-1
, TIMP metallopeptidase inhibitor 1
, Metalloproteinase inhibitor 1
, collagenase inhibitor
, erythroid potentiating activity
, erythroid-potentiating activity
, fibroblast collagenase inhibitor
, metalloproteinase inhibitor 1
, tissue inhibitor of metalloproteinases 1
, tissue inhibitor of metalloproteinase 1 (erythroid potentiating activity, collagenase inhibitor)
, tissue inhibitor of metallopeptidase 1
, tissue inhibitor of metalloproteinase 1
, metalloproteinase tissue inhibitor
, metalloproteinase tissue inhibitor 1
, TPA-induced protein
, collagenase inhibitor 16C8 fibroblast
, tissue inhibitor of metalloproteinase-1