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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 art. Additionally we are shipping Matrix Metallopeptidase 10 (Stromelysin 2) Kits (87) and Matrix Metallopeptidase 10 (Stromelysin 2) Proteins (13) and many more products for this protein.
Showing 10 out of 169 products:
Human Polyclonal MMP10 Primary Antibody for ICC, IHC (fro) - ABIN315644
McCord, Li, Rosewell, Brännström, Curry: Ovarian expression and regulation of the stromelysins during the periovulatory period in the human and the rat. in Biology of reproduction 2012
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Human Polyclonal MMP10 Primary Antibody for WB - ABIN966586
Muller, Quantin, Gesnel, Millon-Collard, Abecassis, Breathnach: The collagenase gene family in humans consists of at least four members. in The Biochemical journal 1988
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Human Polyclonal MMP10 Primary Antibody for ICC, IHC (fro) - ABIN408044
Olivotto, Otero, Astolfi, Platano, Facchini, Pagani, Flamigni, Facchini, Goldring, Borzì, Marcu: IKKα/CHUK regulates extracellular matrix remodeling independent of its kinase activity to facilitate articular chondrocyte differentiation. in PLoS ONE 2013
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Human Polyclonal MMP10 Primary Antibody for WB - ABIN517967
Teng, Wang, Hood, Conrads, Hamilton, Maxwell, Darcy, Conrads: Identification of candidate circulating cisplatin-resistant biomarkers from epithelial ovarian carcinoma cell secretomes. in British journal of cancer 2014
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 (show CXCR4 Antibodies)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 (show CXCR4 Antibodies)/SDF1 (show CXCL12 Antibodies) 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 (show PMP22 Antibodies)) treatment, and conclude MMP10 is required for resolution of DSS (show PMP22 Antibodies)-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.
There is a significant association in the expression of P-Rex1 (show PREX1 Antibodies) 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 (show AJUBA Antibodies) upregulated MMP10 and MMP13 (show MMP13 Antibodies) 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 (show FGA Antibodies) 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 (show MMP7 Antibodies), MMP-10 and TIMP-1 (show TIMP1 Antibodies) correlated with clinicopathologic features. We suggest that these genes may play a role during progression of the disease MMP-10, MMP-7 (show MMP7 Antibodies), TIMP-1 (show TIMP1 Antibodies), TIMP-2 (show TIMP2 Antibodies) 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.
MMP10 expression is significantly upregulated in human masticatory mucosa during wound healing.
Our results suggest that the level of the MMP-10 expression in tumor epithelium of cutaneous squamous cell carcinoma and basal cell carcinoma may contribute to the different invasive patterns observed in these tumors
The present study was aimed to determine the association between metalloproteinase 3 (MMP3 (show MMP3 Antibodies)), transforming growth factor beta 1 (TGFbeta1 (show TGFB1 Antibodies)) and collagen type X alpha I (COL10A1 (show COL10A1 Antibodies)) gene polymorphisms with traits related to leg weakness in pigs.
the identification of MMP1 (show MMP1 Antibodies) and MMP10 genes in swine is reported.
contribution of MMPs to the inflammatory breakdown of the blood-CSF (show CSF2 Antibodies) barrier in vitro
Results indicate that leukemia inhibitory factor (LIF (show LIF Antibodies)) and Oncostatin M (show OSM Antibodies) increase the expression of MMP-1 (show MMP1 Antibodies), MMP-3 (show MMP3 Antibodies), and TIMP-1 (show TIMP1 Antibodies) several fold, and that their expression is reduced to basal levels in the presence of the LIF (show LIF Antibodies) 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