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The protein encoded by MST1 contains four kringle domains and a serine protease domain, similar to that found in hepatic growth factor. Additionally we are shipping MST1 Kits (42) and MST1 Proteins (15) and many more products for this protein.
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Human Monoclonal MST1 Primary Antibody for IF, WB - ABIN968344
Creasy, Chernoff: Cloning and characterization of a human protein kinase with homology to Ste20. in The Journal of biological chemistry 1995
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Human Polyclonal MST1 Primary Antibody for EIA, FACS - ABIN953271
Latiano, Palmieri, Corritore, Valvano, Bossa, Cucchiara, Castro, Riegler, De Venuto, DIncà, Andriulli, Annese: Variants at the 3p21 locus influence susceptibility and phenotype both in adults and early-onset patients with inflammatory bowel disease. in Inflammatory bowel diseases 2010
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Human Polyclonal MST1 Primary Antibody for IHC (p), WB - ABIN392427
Ren, Yan, You, Sun: Down-regulation of mammalian sterile 20-like kinase 1 by heat shock protein 70 mediates cisplatin resistance in prostate cancer cells. in Cancer research 2008
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Study found that MST1 is strongly activated in a diabetic beta cell and induces not only its death but also directly impairs insulin (show INS Antibodies) secretion through promoting proteasomal degradation of key beta cell transcription factor, pancreatic and duodenal homeobox 1 (PDX1 (show PDX1 Antibodies)), which is critical for insulin (show INS Antibodies) production.
deacetylation of MST1 mediated by HBXIP-enhanced HDAC6 results in MST1 degradation in a chaperone-mediated autophagy (CMA) manner in promotion of breast cancer growth.
Mst1 increases the (show FOXP3 Antibodies)acetylation of Foxp3 by inhibiting Sirt1 activity, which requires the Mst1 kinase activity.
Identify MST1/MSP as a mitogen for tracheal basal cells.
MSP (show MSMB Antibodies) appears to promote the migration of fibroblasts, enhances collagen synthesis and remodeling, and effectively improves wound healing.
Elevated serum levels of MST1 were found in subjects with excessive alcohol use.
results suggest that the decreased expression of MST1 in regulatory T cells due to hypermethylation of the promoter contributes to the pathogenesis of IgG4-related AIP (show AIP Antibodies)
Results suggest that Mst1 regulates proliferation of glioma cells via AKT (show AKT1 Antibodies)/mTOR (show FRAP1 Antibodies) signaling pathway
Hippo and Yap (show YAP1 Antibodies) regulate cardiomyocyte death and regeneration.
MST1 protein gene expression is a prognostic indicator for patients diagnosed with colorectal cancer.
Using a standard two-thirds partial hepatectomy (PH) model in young and aged mice, the activity of the core kinases MST1 and LATS1 (show LATS1 Antibodies) increased during the early hypertrophic phase and returned to steady state levels in the proliferative phase, coinciding with activation of YAP1 (show YAP1 Antibodies) target genes and hepatocyte proliferation.
The MST1 acts as a molecular brake to maintain immune tolerance by regulating T cell-mediated B cell activation (show BLNK Antibodies).
Mst1 knockout alleviated while Mst1 overexpression aggravated cardiac dysfunction in diabetes.
these findings highlight a role for MST1 in vesicle trafficking and extravasation in neutrophils, providing an additional mechanistic explanation for the severe immune defect
Results identify L-plastin (show LCP1 Antibodies) as a key effector of Mst1 and establish a novel mechanism linking a signaling intermediate to an actin-binding protein (show PFN1 Antibodies) critical to T cell migration.
MIST1 is a scaling factor necessary and sufficient by itself to induce and maintain secretory cell architecture
Mst1 deficiency diminishes atherosclerosis and stabilizes atherosclerotic plaques in ApoE (show APOE Antibodies)(-/-) mice. Mst1 may participate in atherosclerosis progression through inhibition of macrophage autophagy and promotion of macrophage apoptosis.
These results suggest that melatonin alleviates postinfarction cardiac remodeling and dysfunction by upregulating autophagy, decreasing apoptosis, and modulating mitochondrial integrity and biogenesis. The attributed mechanism involved, at least in part, Mst1/Sirt1 (show SIRT1 Antibodies) signaling
TRAF2 (show TRAF2 Antibodies) functions as a key activator of MST1 in oxidative stress-induced (show SQSTM1 Antibodies) intracellular signaling processes.
Mst1 regulates hepatic lipid metabolism by inhibiting Sirt1 (show SIRT1 Antibodies) ubiquitination in mice.
The protein encoded by this gene contains four kringle domains and a serine protease domain, similar to that found in hepatic growth factor. Despite the presence of the serine protease domain, the encoded protein may not have any proteolytic activity. The receptor for this protein is RON tyrosine kinase, which upon activation stimulates ciliary motility of ciliated epithelial lung cells. This protein is secreted and cleaved to form an alpha chain and a beta chain bridged by disulfide bonds.
hepatocyte growth factor-like protein
, hepatocyte growth factor-like protein homolog
, macrophage-stimulating protein
, macrophage stimulatory protein
, E2F transcription factor 2
, hepatocyte growth factor-like/macrophage stimulating protein