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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.
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Human Polyclonal MMP20 Primary Antibody pour IF (p), IHC (p) - ABIN714761
Ogbureke, Koli, Saxena: Matrix Metalloproteinase 20 Co-expression With Dentin Sialophosphoprotein in Human and Monkey Kidneys. dans The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2016
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The article data showed that MMP20 rs1784418 C>T (Matrix metalloproteinase 20) appears to protect against dental caries, but its effects are likely to be more marked in certain populations.
DSPP (Montrer DSPP Anticorps)-MMP20 pair may play a role in the normal turnover of cell surface proteins and/or repair of pericellular matrix proteins of the basement membranes in the metabolically active duct epithelial system of the nephrons.
Levels of matrix metalloproteinases MMP-19 (Montrer MMP19 Anticorps) and MMP-20 expression are significantly increased in pancreatic ductal adenocarcinoma (PDAC).
The expression of MMP20 was lower in calcifying cystic odontogenic tumor when compared to all tumors and cysts.
The growth of choroidal neovascularization in AMD (Montrer AMD1 Anticorps) would be affected by 2 genes: MMP20, a newly confirmed gene expressed in the retina, and ARMS2 (Montrer ARMS2 Anticorps)/HTRA1 (Montrer HTRA1 Anticorps), a well-known susceptibility gene for AMD (Montrer AMD1 Anticorps).
Novel homozygous mutation MMP20 (c.1054G>A, p.Glu352Lys) genes were identified in amelogenesis imperfect consanguinity. Mutant MMP20 was expressed at a normal level but secreted only minimally with proteolytic function.
expression of MMP-20 and co-expression and potential interaction with DSPP (Montrer DSPP Anticorps) in human major salivary gland tissues
The results identify MMP-20 as a broad activator of pro-KLKs, suggesting the potential for intersection of the KLK and MMP axes under pathological dysregulation of MMP-20 expression.
Polymorphisms of MMP7 (Montrer MMP7 Anticorps) and MMP20 genes may be surrogate markers to predict long-term outcomes after kidney transplantation.
mineralized content slightly decreased; magnesium substituting for calcium in crystal. anomalies affected enamel with minimal interrod enamel; apatite crystals perpendicular to enamel prisms, suggesting possible new role for MMP20 in enamel formation.
MMP20 in a common ancestor of tetrapods might have been recruited for the processing of AMEL (Montrer AMELX Anticorps) and conserved over 350 million years of evolution.
MMP-20 is the enzyme that processes ameloblastin (Montrer AMBN Anticorps) during the secretory stage of amelogenesis
MMP-20 processes dental sialophosphoprotein into smaller subunits in the dentin matrix during odontogenesis
increased cadherin cleavage by transgenic MMP20 in the wild type background releases excess beta-catenin (Montrer CTNNB1 Anticorps), which translocates to ameloblast nuclei to promote cell migration/invasion. Therefore, MMP20 plays a role in normal ameloblast migration through tightly controlled Wnt (Montrer WNT2 Anticorps) signaling and MMP20 overexpression disrupts this process.
MMP-20 action guides the growth morphology of the forming hydroxyapatite crystals and enhances their crystallinity.
Matrix metalloproteinase-20 over-expression is detrimental to enamel development
MMP20 cleaves extracellular domains of cadherin adherens junction proteins, both E- and N-cadherin (Montrer CDH2 Anticorps) transcripts are expressed at significantly higher levels in Mmp20 null mice; in Mmp20 ablated mice N-cadherin (Montrer CDH2 Anticorps) expression persists during maturation stage
enamel of M180Tg/AmelxKO mice was thinner than WT, it had similar mechanical properties and decussating enamel prisms, which were abolished by the loss of MMP20 in the M180Tg/DKO mice.
MMP20 may influence ameloblast developmental progression through hydrolysis of cadherin extracellular domains with associated release of transcription factor(s).
Effect of kallikrein 4 (Montrer KLK4 Anticorps) loss on enamel mineralization: comparison with mice lacking matrix metalloproteinase 20.
Runx2 (Montrer RUNX2 Anticorps) regulates the expression of ODAM (Montrer ODAM Anticorps) and nuclear ODAM (Montrer ODAM Anticorps) serves an important regulatory function in the mineralization of enamel through the regulation of MMP-20 apart from a different, currently unidentified, function of extracellular ODAM (Montrer ODAM Anticorps).
expression of MMP-20 correlates with the stage-associated changes in the digestion of enamel proteins
enamelysin activity is essential for proper enamel development in mice
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 degrades amelogenin, the major protein component of dental enamel matrix, and thus thought to play a role in tooth enamel formation. A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta. This gene is part of a cluster of MMP genes located on chromosome 11q22.3.
, matrix metalloproteinase 20 (enamelysin)
, matrix metalloproteinase-20
, matrix metallopeptidase 20 (enamelysin)
, matrix metallopeptidase 25
, matrix metallopeptidase 20
, matrix metalloproteinase 20
, matrix metalloproteinase