Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
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 10 (Stromelysin 2) Antikörper (184) und Matrix Metallopeptidase 10 (Stromelysin 2) Kits (93) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 16 products:
Human MMP10 Protein expressed in Escherichia coli (E. coli) - ABIN1080259
Zheng, Hu, Huang, Xu, Yang, Li: In vivo bioengineered ovarian tumors based on collagen, matrigel, alginate and agarose hydrogels: a comparative study. in Biomedical materials (Bristol, England) 2015
These results indicate that MMP10 serves a beneficial role in response to acute infection by moderating the proinflammatory response of resident and infiltrating macrophages.
MMP-10 facilitates the clearance of multiwalled carbon nanotubesand moderates the pro-inflammatory response of exposed alveolar and infiltrated macrophages.
crosstalk between MMP10 and the CXCR4/SDF1 axis contributes to hepatocarci (zeige CXCR4 Proteine)nogenesis
Matrix metalloproteinase-10 expression is induced during hepatic injury and plays a fundamental role in liver tissue repair.
our findings support a model in which MMP-10 activity modulates CXCR4 (zeige CXCR4 Proteine)/SDF1 (zeige CXCL12 Proteine) signaling, which is essential for efficient skeletal muscle regeneration.
Dissection of the matrix metalloproteinase 10 (MMP10) substrate degradome in fibroblast secretomes.
Thus, our findings indicate that MMP-10 is critical for skeletal muscle maintenance and regeneration during injury and disease.
MMP10 promotes macrophage movement
Assessed MMP-10's role in a murine model of colonic tissue damage induced by dextran sulfate sodium(DSS (zeige PMP22 Proteine)) treatment, and conclude MMP10 is required for resolution of DSS (zeige PMP22 Proteine)-induced colonic damage, and in its absence, chronic inflammation and dysplasia occurs.
Mmp10 is required for maintenance of a highly tumorigenic, cancer-initiating, metastatic stem-like cell population in lung cancer.
increased abundance of Snail (zeige SNAI1 Proteine) and Axin2 (zeige AXIN2 Proteine) is highly correlated to malignant transformation of OL, making them novel biomarker(s) predicting oral cancer development
MMP10, either alone or in combination with tPA (zeige PLAT Proteine), might represent a new strategy for thrombolysis in ischemic stroke, providing higher protection against cerebrovascular damage.
There is a significant association in the expression of P-Rex1 and MMP10 in human luminal breast cancer, and their co-expression is indicative of poor prognosis.
MMP10 is a novel marker for cancer stem-like cells (CSCs)/cancer-initiating cells in epithelial ovarian cancer
Data show that AJUBA (zeige AJUBA Proteine) upregulated MMP10 and MMP13 (zeige MMP13 Proteine) expression in esophageal squamous cell carcinoma (ESCC).
MMP10 is overexpressed in the serum and pulmonary arteries of patients with systemic sclerosis-associated pulmonary hypertension.
Using a quantum chemical approach method, it has been established that mutations in MMP-10 and FGA (zeige FGA Proteine) proteins led to substantial energetic modifications suggesting an impact on their functions and/or stability in the recurrent pregnancy loss patients.
We conclude that in the resected esophageal cancer an increased mRNA expression of MMP-7 (zeige MMP7 Proteine), MMP-10 and TIMP-1 (zeige TIMP1 Proteine) correlated with clinicopathologic features. We suggest that these genes may play a role during progression of the disease MMP-10, MMP-7 (zeige MMP7 Proteine), TIMP-1 (zeige TIMP1 Proteine), TIMP-2 (zeige TIMP2 Proteine) were overexpressed in 73%, 85%, 55% and 42% of esophageal cancer samples, respectively.
Mycobacterium tuberculosis activates inflammatory and stromal cells to secrete MMP-10, and this is partly driven by the virulence factor early secretory antigenic target-6.
The present study was aimed to determine the association between metalloproteinase 3 (MMP3 (zeige MMP3 Proteine)), transforming growth factor beta 1 (TGFbeta1 (zeige TGFB1 Proteine)) and collagen type X alpha I (COL10A1 (zeige COL10A1 Proteine)) gene polymorphisms with traits related to leg weakness in pigs.
the identification of MMP1 (zeige MMP1 Proteine) and MMP10 genes in swine is reported.
contribution of MMPs to the inflammatory breakdown of the blood-CSF (zeige CSF2 Proteine) barrier in vitro
Results indicate that leukemia inhibitory factor (LIF (zeige LIF Proteine)) and Oncostatin M (zeige OSM Proteine) increase the expression of MMP-1 (zeige MMP1 Proteine), MMP-3 (zeige MMP3 Proteine), and TIMP-1 (zeige TIMP1 Proteine) several fold, and that their expression is reduced to basal levels in the presence of the LIF (zeige LIF Proteine) antagonist MH35-BD.
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 proteoglycans and fibronectin. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3.
matrix metalloproteinase 10
, matrix metalloproteinase-10
, stromelysin 2
, matrix metalloprotease 10
, matrix metalloproteinase 10 (stromelysin 2)
, transin 2
, transformation-associated protein 34A
, matrix metalloproteinase 3