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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 25 Kits (17) und und viele weitere Produktgruppen zu diesem Protein an.
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Human Monoclonal MMP25 Primary Antibody für CyTOF, FACS - ABIN4900198
Zhao, Sohail, Sun, Shi, Kim, Mobashery, Fridman: Identification and role of the homodimerization interface of the glycosylphosphatidylinositol-anchored membrane type 6 matrix metalloproteinase (MMP25). in The Journal of biological chemistry 2008
Show all 2 Pubmed References
In absolute mRNA levels, significant differences were found in expression of MMP2, MMP24, and MMP25 in gastric carcinoma compared with superficial gastritis.
IL-2 (zeige IL2 Antikörper)-upregulated MT6 (zeige PRSS33 Antikörper) cell-surface expression correlates with CD16 (zeige CD16 Antikörper) downmodulation. MT6 (zeige PRSS33 Antikörper), sequestered in intracellular compartments in unstimulated NK cells, translocates to the effector-target cell interface of CD16 (zeige CD16 Antikörper)-mediated immunological synapses.
MT6-MMP regulates neutrophil and monocyte chemotaxis and by generating "eat-me" signals upon vimentin (zeige VIM Antikörper) cleavage potentially increases phagocytic removal of neutrophils to resolve inflammation.
individuals with history of chronic airways inflammation (asthma and COPD (zeige ARCN1 Antikörper)) serum leukolysin may be a metabolic marker associated with chronic atopy-associated respiratory inflammation.
MMP25 (zeige MMP24 Antikörper) is regulated by clusterin (zeige CLU Antikörper) in vivo
MMP-25 plays an important role in multiple sclerosis pathology
this study shows that Mmp25-null mice exhibit a defective innate immune response characterized by low sensitivity to bacterial LPS (zeige TLR4 Antikörper), hypergammaglobulinemia, and reduced secretion of proinflammatory molecules
These data suggest MMP-25 is a direct transcriptional target for TGF-beta3 (zeige TGFB3 Antikörper) in mouse secondary palate development and could be a target for TGF-beta3 (zeige TGFB3 Antikörper) elsewhere as well.
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 MMPs are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily, attached to the plasma membrane via a glycosylphosphatidyl inositol anchor. In response to bacterial infection or inflammation, the encoded protein is thought to inactivate alpha-1 proteinase inhibitor, a major tissue protectant against proteolytic enzymes released by activated neutrophils, facilitating the transendothelial migration of neutrophils to inflammatory sites. The encoded protein may also play a role in tumor invasion and metastasis through activation of MMP2. The gene has previously been referred to as MMP20 but has been renamed MMP25.
, matrix metallopeptidase-like 1
, matrix metalloproteinase 20
, matrix metalloproteinase 25
, matrix metalloproteinase-25
, matrix metalloproteinase-like 1
, membrane-type 6 matrix metalloproteinase
, membrane-type matrix metalloproteinase 6
, membrane-type-6 matrix metalloproteinase
, LOW QUALITY PROTEIN: matrix metalloproteinase-25