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Human MGLL Protein expressed in Escherichia coli (E. coli) - ABIN667833
Nomura, Long, Niessen, Hoover, Ng, Cravatt: Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis. in Cell 2010
Show all 2 references for ABIN667833
Human MGLL Protein expressed in Wheat germ - ABIN1310880
Bolen, Naren, Yarlagadda, Beranova-Giorgianni, Chen, Norman, Baker, Rowland, Best, Sano, Tsukahara, Liliom, Igarashi, Tigyi: The phospholipase A1 activity of lysophospholipase A-I links platelet activation to LPA production during blood coagulation. in Journal of lipid research 2011
the presence and differential distribution of fatty acid amide hydrolase (FAAH (show FAAH Proteins)) and monoglyceride lipase (MGLL) in relation to CB1 (show CNR1 Proteins) during the maturation of human oocytes, was investigated.
there was evidence that MGLL rs604300 genotype interacts with early life adversity to predict threat-related basolateral amygdala habituation, a neural phenotype linked to the endocannabinoid system and addiction
This study unravels a novel mechanism of SND1 (show SND1 Proteins) function and identifies MGLL as a unique tumor suppressor for HCC (show FAM126A Proteins). MGLL might function as a homeostatic regulator of Akt (show AKT1 Proteins) restraining its activation.
Monoacylglycerol lipase sulfenylation might act as an intrinsic neuroprotective mechanism by potentiating 2-AG signaling at CB1 (show CNR1 Proteins) receptors.
The study identified monoacylglycerol lipase as a YAP (show YAP1 Proteins) transcriptional target and an inhibitor of anchorage-dependent cell growth.
Molecular dynamics and nudged elastic band simulations were used to explore the conformational transition pathway of the helix alpha4 of human monoacylglycerol lipase.
role of monoacylglycerol lipase (MAGL) in the cancer progress
Our findings establish that MAGL promotes metastases in nasopharyngeal carcinoma
In subcutaneous adipose tissue, DAGL-a mRNA was upregulated and fatty acid amide hydrolase (FAAH (show FAAH Proteins)) and monoacylglycerol lipase (MAGL) mRNAs were down-regulated in obese subjects, but the diets had no influence.
In obese humans, FAAH (show FAAH Proteins) or MGL (show CLEC10A Proteins) activity in adipocytes is not affected by diabetes, dyslipidaemia or other markers of metabolic dysfunction.
Activities of adipose triglyceride lipase (ATGL (show PNPLA2 Proteins)), hormone sensitive lipolitic enzyme (HSL (show LIPE Proteins)) and monoacylglycerol lipase (MGL) were significantly higher (51 %, 38 %, 49 %) in the DE group than the HF group (p < 0.05). MGL (show CLEC10A Proteins), there were no differences between the CO group, HF group, and DC group, with the DE group (70 %) being significantly higher (p < 0.05).
MGL (show CLEC10A Proteins) in astrocytes is an important regulator of 2-arachidonoylglyerol levels, arachidonic acid availability, and neuroinflammation.
Genetic and pharmacological ablation of Magl attenuated centrally-mediated fever response.
the results indicate that global MGL (show CLEC10A Proteins) deletion leads to systemic changes that produce a leaner (show CACNA1A Proteins) phenotype and an improved serum metabolic profile.
This study showed that Genetic deletion of monoacylglycerol lipase leads to impaired cannabinoid receptor CBR (show CBR1 Proteins) signaling and anxiety-like behavior.
Suggest that organophosphate agents induce plasma hypertriglyceridemia in mouse through single or dual inhibition of FAAH (show FAAH Proteins) or/and MAGL, apparently leading to overstimulation of cannabinoid signal regulating energy metabolism.
Inactivation of Monoacylglycerol lipase robustly suppressed production and accumulation of beta-amyloid (Abeta (show APP Proteins)) associated with reduced expression of beta-site amyloid precursor protein cleaving enzyme 1 (BACE1 (show BACE Proteins)) in a mouse model of Alzheimer's disease.
Data indicate that nerve growth factor (NGF) controls monoacylglycerol lipase (MGL) degradation in vitro and in vivo.
The results therefore suggest a role for intestinal MGL (show CLEC10A Proteins) in whole body energy balance via regulation of food intake as well as metabolic rate.
MGL (show CLEC10A Proteins) regulates 2-arachidonoylglycerol signaling rather broadly within a certain range of neural tissue, although MGL (show CLEC10A Proteins) expression is heterogeneous and limited to a subset of nerve terminals and astrocytes.
This gene encodes a serine hydrolase of the AB hydrolase superfamily that catalyzes the conversion of monoacylglycerides to free fatty acids and glycerol. The encoded protein plays a critical role in several physiological processes including pain and nociperception through hydrolysis of the endocannabinoid 2-arachidonoylglycerol. Expression of this gene may play a role in cancer tumorigenesis and metastasis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
, Monoglyceride lipase
, lysophospholipase homolog
, monoacylglycerol lipase