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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. Zusätzlich bieten wir Ihnen Matrix Metallopeptidase 13 (Collagenase 3) Kits (145) und Matrix Metallopeptidase 13 (Collagenase 3) Proteine (41) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 290 products:
Human Polyclonal MMP13 Primary Antibody für IF (p), IHC (p) - ABIN670341
Luo, Zhang, Wang, Hu, Song, Su, Zhang: Alendronate retards the progression of lumbar intervertebral disc degeneration in ovariectomized rats. in Bone 2013
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Cow (Bovine) Polyclonal MMP13 Primary Antibody für IP, IHC - ABIN223238
Spinale, Escobar, Mukherjee, Zavadzkas, Saunders, Jeffords, Leone, Beck, Bouges, Stroud: Cardiac-restricted overexpression of membrane type-1 matrix metalloproteinase in mice: effects on myocardial remodeling with aging. in Circulation. Heart failure 2009
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Human Monoclonal MMP13 Primary Antibody für IF, IHC - ABIN4334944
Huang, Ao, Li, Wu, Xu, Deng, Chen, Yin, Cheng: Autophagy Protects Advanced Glycation End Product-Induced Apoptosis and Expression of MMP-3 and MMP-13 in Rat Chondrocytes. in BioMed research international 2017
Cow (Bovine) Polyclonal MMP13 Primary Antibody für ICC, IF - ABIN4334942
Ma, Liu, Wang, Chen, Liu, Li, Xiang, Wei, Duan, Han: Tamoxifen induces the development of hernia in mice by activating MMP-2 and MMP-13 expression. in Biochimica et biophysica acta 2015
Cow (Bovine) Polyclonal MMP13 Primary Antibody für WB - ABIN2786656
Borghese, Chiche, Vernerey, Chenot, Mir, Bijaoui, Bonaiti-Pellié, Chapron: Genetic polymorphisms of matrix metalloproteinase 12 and 13 genes are implicated in endometriosis progression. in Human reproduction (Oxford, England) 2008
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Rat (Rattus) Polyclonal MMP13 Primary Antibody für ICC, IHC - ABIN1172288
Chu, Dai, Wang, Tian, Song, Xiao, Shao, Zhang, Zhang: Strontium ranelate causes osteophytes overgrowth in a model of early phase osteoarthritis. in BMC musculoskeletal disorders 2017
One important finding of the present study was that MMP-3 (zeige MMP3 Antikörper) appears to be involved solely in early-onset preeclampsia, but not in late-onset preeclampsia. Higher levels of MMP-2 (zeige MMP2 Antikörper) and MMP-13 and lower levels of MMP-9 (zeige MMP9 Antikörper) seem to be related to both early- and late-onset severe preeclampsia.
Transfection of cells with either miR (zeige MLXIP Antikörper)-100 or miR (zeige MLXIP Antikörper)-125b negated the induction of MMP13 release. Additionally, AR activation induced a morphological alteration of MDA-MB-453 cells, which was blocked by miR (zeige MLXIP Antikörper)-125b only.
ATM (zeige ATM Antikörper) could be activated by lung cancer-associated TNF-alpha (zeige TNF Antikörper), up-regulate MMP-13 expression and thereby augment tumor metastasis
The Sp1 (zeige PSG1 Antikörper)-mediaded allelic regulation of MMP13 expression by an esophageal squamous cell carcinoma susceptibility SNP rs2252070 has been demonstrated.
MMP-13 IRS (zeige IARS Antikörper) represents a suitable method to assess pathologic grade of precancerous and cancerous colorectal lesions. MMP-13 has been identified as an excellent marker of high grade IEN and CRC (zeige CALR Antikörper), and may thus be applied for prognostic stratification.
These findings suggest that using MMP-13 inhibitors in diffuse group might contribute to the control of tumor growth
The present results suggested that Icariin may have a chondroprotective effect, exerted through the inhibition of MMP1 (zeige MMP1 Antikörper), MMP3 (zeige MMP3 Antikörper) and MMP13 via MAPK (zeige MAPK1 Antikörper) pathways. Therefore, Icariin may have potential as a novel therapeutic strategy for the treatment of osteoarthritis.
MMP-13 may play a role on physiological turnover of cartilage extracellular matrix and that LRP1 (zeige LRP1 Antikörper) is a key modulator of extracellular levels of MMP-13 and its internalization is independent of the levels of ADAMTS-4 (zeige ADAMTS4 Antikörper), -5 and TIMP-3 (zeige TIMP3 Antikörper).
proteolysis of collagen-rich natural extracellular matrix (ECM (zeige MMRN1 Antikörper)), performed uniquely by individual homologous proteases, leads to distinct events that eventually affect overall ECM (zeige MMRN1 Antikörper) morphology, viscoelastic properties, and molecular composition.
A strong association between the -77 MMP-13 polymorphism and posterior tibial tendinopathy insufficiency.
that MMP-13 is a central protease in infarct development and cortical remodeling during post-stroke neurorepair
the phenotype seen in the Hdac4 (zeige HDAC5 Antikörper)(-/-) mice is partially derived from elevation in MMP-13 and may be due to a bone remodeling disorder caused by overexpression of this enzyme.
MEF2C (zeige MEF2C Antikörper) is necessary for Mmp13 gene expression at the transcriptional level and participates in PTH (zeige PTH Antikörper)-stimulated Mmp13 gene expression by increased binding to c-FOS at the AP-1 (zeige JUN Antikörper) site in the Mmp13 promoter.
data reveal a novel involvement of MMP-13 in regulating dendritic cell (DC) immunobiology through moderating MHC-I surface presentation, endocytosis and cytokine/chemokine (zeige CCL1 Antikörper) secretion; furthermore, the reduced MHC-I surface presentation by DCs resulted in a poor CD8 (zeige CD8A Antikörper)(+) T-cell response in vitro; MMP-13 might be a promising target for therapeutic intervention in inflammatory diseases
The progressive process of articular cartilage degeneration was significantly delayed in the knee joints of Ddr2 (zeige DDR2 Antikörper)-deficient mice in comparison to their control littermates. Articular cartilage damage in the knee joints of the mice was associated with increased expression profiles of both Ddr2 (zeige DDR2 Antikörper) and matrix metalloproteinase 13.
Postnatal chondrocyte-specific deletion of Hdac3 (zeige HDAC3 Antikörper) with an inducible Col2a1 (zeige COL2A1 Antikörper)-Cre caused premature production of pErk1/2 and Mmp13 in the growth plate.
Mmp13 is selectively regulated of by 1,25-Dihydroxyvitamin D3, PTH (zeige PTH Antikörper), and Osterix (zeige SP7 Antikörper) through distal enhancers.
Our study contributes to the understanding of the role of HIF1alpha (zeige HIF1A Antikörper) in OA and highlights the HIF1alpha (zeige HIF1A Antikörper)-beta-catenin (zeige CTNNB1 Antikörper) interaction, thus providing new insights into the impact of hypoxia in articular cartilage.
Matrix metalloproteinases (MMP) are effectors of hippocampal neuroplasticity in the adult central nervous system and that the MMP-1 (zeige MMP1 Antikörper)/protease-activated receptor-1 (zeige F2R Antikörper) axis may play a role in neurogenesis following physiological and/or pathological stimuli.
IL-1Ra (zeige IL1RN Antikörper) is associated with MMP-13 expression and has a novel function in such regulation without interference of the IL-1 (zeige IL1A Antikörper) signaling cascade.
p38 (zeige MAPK14 Antikörper) phosphorylation and MMP13 expression are regulated by Rho/ROCK activation, and support the potential novel pathway that Rho/ROCK is in the upper part of the mechanical stress-induced matrix degeneration cascade in cartilage.
These data identify atypical PKC isozymes as STAT and ERK activators that mediate c-fos and collagenase expression.
MMP-13 treatment of fresh articular cartilage results in cleaved fibromodulin (zeige FMOD Antikörper) fragments
increased in bovine preovulatory follicles following the gonadotropin surge but no up-regulation of MMP-1 (zeige MMP1 Antikörper) and MMP-13 (follicular apex (zeige APEX1 Antikörper) vs. base) for the preovulatory collagenolysis required for follicle rupture
involvement of p38 MAP kinase (zeige MAPK14 Antikörper) in the hyaluronan oligosaccharide induction of MMP-13
MMP-13 and collagenase have roles in chondrocyte hypertrophy induced by type II collagen (zeige COL2A1 Antikörper)
At high but naturally occurring concentrations the collagen peptide CB12 (zeige PABPC4 Antikörper)-II induced an increase in the expressions of MMP-13 and cleavage of type II collagen (zeige COL2A1 Antikörper) by collagenase in the mid zone and also in the superficial zone.
XCL3 and XCL4 can be differentially induced by prolactin (zeige PRL Antikörper) and thyroid hormone (zeige PTH Antikörper)(3)
MeHg impairs tail development at least partially by activation of the tissue remodeling proteases Mmp9 (zeige MMP9 Antikörper) and Mmp13.
Zebra fish embryogenesis requires MMP-13 and dexamethasone and hydrocortisone modulate the expression of this gene, leading to increased activity and potentially contributing to subsequent dysmorphogenesis.
JNK (zeige MAPK8 Antikörper)-Mmp13 signaling pathway plays an essential role in regulating the innate immune cell migration in response to severe injury in vivo
These results suggest that PEP-1-SIRT2 (zeige SIRT2 Antikörper) promotes matrix metalloproteinases-induced dedifferentiation via ERK (zeige MAPK1 Antikörper) signaling in articular chondrocytes.
chitosan-pDNA nanoparticles encoding shRNA targeting MMP-3 (zeige MMP3 Antikörper) and -13 had great potential in silencing the dedifferentiation-related genes for regenerating prolonged and endurable cartilage.
Leptin (zeige LEP Antikörper) can induce MMP-13 and have a synergistic induction effect on NO with TNF-alpha (zeige TNF Antikörper) in rabbit articular chondrocytes in vitro.
The DNA microarray analysis for matrix metalloproteinase (MMP)-related mRNA expression in equine superficial digital flexor tendinitis indicated that mRNA level of MMP-13 was apparently up-regulated in the tendinitis as compared to normal tendon.
TNF-alpha (zeige TNF Antikörper) induced MMP-13 expression by condylar cells might be involved in the degradation of the juvenile condyle.
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 protein encoded by this gene cleaves type II collagen more efficiently than types I and III. It may be involved in articular cartilage turnover and cartilage pathophysiology associated with osteoarthritis. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3.
, collagenase 3
, matrix metalloproteinase 13 (collagenase 3)
, interstitial collagenase
, matrix metalloproteinase 13
, matrix metalloproteinase-13
, gene 11
, matrix metallopeptidase 13 (collagenase 3)
, gene A
, collagenase 3-like