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The protein encoded by PTGES is a glutathione-dependent prostaglandin E synthase. Additionally we are shipping Prostaglandin E Synthase Antibodies (56) and Prostaglandin E Synthase Proteins (6) and many more products for this protein.
Showing 7 out of 21 products:
Human Prostaglandin E Synthase ELISA Kit for Sandwich ELISA - ABIN417308
Yu, Hou, Sun, Liu, Li et al.: Upregulation of C-C chemokine receptor type 7 expression by membrane-associated prostaglandin E synthase-1/prostaglandin E2 requires glycogen synthase kinase 3β-mediated signal transduction in colon ... in Molecular medicine reports 2015
The identified amino acid residues can act as target sites for the design and development of drug candidates against mPGES-1
These findings support the value of a prognostic and predictive role for mPGES1.
Data show that statins limit hepatic myofibroblasts proliferation via a cyclooxyegnase-2 (COX-2 (show COX2 ELISA Kits)) and microsomal PGE (show LIPF ELISA Kits) synthase-1 (mPGES-1) dependent pathway.
Data show that cyclooxygenase2 (COX2 (show COX2 ELISA Kits))overexpression induces prostaglandin E synthase (PTGES) through early growth response 1 (EGR1 (show EGR1 ELISA Kits)) in colorectal cancer cell lines.
mPGES-1 is downregulated via EGR1 (show EGR1 ELISA Kits) and has a role in caffeine inhibition on PGE2 synthesis of HBx hepatocytes
results demonstrate that mPGES-1 is a target gene of defective mismatch repair in human colorectal cancer, with functional consequence
Altered expression of EP2 in patients with aspirin-exacerbated respiratory disease contributes to deficient induction of IL-1RI, reducing the capacity of IL-1beta (show IL1B ELISA Kits) to increase COX-2 (show COX2 ELISA Kits) and mPGES-1 expression, which results in low PGE2 production
High levels of intra tumoral mPGES-1 is associated with poor prognosis. mPGES-1 after chemotherapy is associated with improved outcomes.
mPGES-1 in prostate cancer controls stemness and amplifies epidermal growth factor receptor (show EGFR ELISA Kits)-driven oncogenicity
we investigated the changes in promoter methylation patterns using methylation arrays and observed that the promoters of immunomodulatory factors, COX2 (show COX2 ELISA Kits) and PTGES, and migration-related factors, CXCR2 (show CXCR2 ELISA Kits) and CXCR4 (show CXCR4 ELISA Kits), were hypomethylated after 5-aza treatment
mPges-1 depletion modestly increased thrombogenesis in LDL-receptor (show LDLR ELISA Kits) knockout mice. This response was markedly further augmented by coincident deletion of the I prostanoid receptor.
Data (including data from studies in knockout mice) suggest interactions of cholinergic/prostaglandin systems participate in neuroimmunomodulation; microsomal Ptges-1 is part of cholinergic anti-inflammatory response in chronic inflammatory diseases.
Prostacyclin synthase (show PTGIS ELISA Kits) and prostaglandin E synthase-1 cooperatively exacerbate inflammatory reactions but have opposing effects on carcinogenesis.
Gas6 (show GAS6 ELISA Kits), through upregulation of Ptges/PGE2, contributes to cancer-induced venous thrombosis.
Vascular mPGES-1 plays a protective role in blood vessels and attenuates rupture of cerebral aneurysms.
Suggest pivotal role of COX-2 (show COX2 ELISA Kits)-mPGES-1-PGE2 axis in vascular calcification. Inhibition of COX-2 (show COX2 ELISA Kits) or mPGES-1 may increase the risk of calcification and subsequent adverse cardiovascular events during chronic renal failure.
The present results suggest that mPGES-1 plays a significant role in lymphangiogenesis during inflammation, and represents a novel target for controlling IL.
data suggests that an as yet unidentified prostaglanind E synthase but not mPGES-1 may couple with COX-2 (show COX2 ELISA Kits) to mediate increased renal PGE2 sythsesis in DN.
This study shown that mPGES-1 is expressed in the mouse brain, both in vascular endothelial cells, in several other cellular of capillary associated pericytes, astrocytes, and cells in circumventricular organs, choroid plexus, and leptomeninges.
mPGES-1 deficiency exacerbates bleomycin-induced pulmonary fibrosis.
Prostaglandin E synthase interacts with inducible heat shock protein 70 (show HSPA1A ELISA Kits) after heat stress in bovine primary dermal fibroblast cells.
Messenger RNA and protein levels of prostaglandin (PG) E synthase (PGES), PGF2alpha receptor (PGFR), tumor necrosis factor-alpha (TNF (show TNF ELISA Kits)) and Fas (show FAS ELISA Kits) were found to be higher in the corpus luteum of pregnancy than in corpus luteum of the cycle.
Data suggest that elevated temperatures stimulate PGE2 production in ampullary oviduct by increasing expression of PGES and HSP90AA1 (show HSP90AA1 ELISA Kits) (heat shock 90 kD protein 1 alpha).
PGES pathway is responsible for the endometrial production of PGE (show LIPF ELISA Kits)(2) in the bovine endometrium during the estrous cycle
This study showed that COX-1 (show PTGS1 ELISA Kits) and COX-2 (show PTGS2 ELISA Kits) in genital carcinomas in the horse is poor; microsomal PGES-1 is more prominently expressed.
The protein encoded by this gene is a glutathione-dependent prostaglandin E synthase. The expression of this gene has been shown to be induced by proinflammatory cytokine interleukin 1 beta (IL1B). Its expression can also be induced by tumor suppressor protein TP53, and may be involved in TP53 induced apoptosis. Knockout studies in mice suggest that this gene may contribute to the pathogenesis of collagen-induced arthritis and mediate acute pain during inflammatory responses.
microsomal prostaglandin E synthase-1
, prostaglandin E synthase
, MGST1-like 1
, glutathione S-transferase 1-like 1
, microsomal glutathione S-transferase 1-like 1
, microsomal prostaglandin E synthase 1
, p53-induced apoptosis protein 12
, p53-induced gene 12 protein
, tumor protein p53 inducible protein 12