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The enzyme encoded by GLO1 is responsible for the catalysis and formation of S-lactoyl-glutathione from methylglyoxal condensation and reduced glutatione. Zusätzlich bieten wir Ihnen Glyoxalase I Antikörper (152) und Glyoxalase I Kits (32) und viele weitere Produktgruppen zu diesem Protein an.
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This study shows that only the GLO1 C-7T polymorphism, and not the GLO1 A419C and ALR (zeige GFER Proteine) C-106T polymorphisms, is associated with carotid atherosclerosis in Chinese patients with type 2 diabetes.
The expression of glyoxalase system member glyoxalase 1 (GLO1) in melanoma cells is downregulated by miR (zeige MLXIP Proteine)-137. siRNA targeting of GLO1 mimicks inhibition of melanoma cell proliferation caused by miR (zeige MLXIP Proteine)-137 overexpression. Re-expression of GLO1 restores miR (zeige MLXIP Proteine)-137-mediated suppression of melanoma cell proliferation.
The critical role of glyoxalases as regulators of tumorigenesis in the prostate through modulation of various critical signaling pathways, and an overview of the current knowledge on glyoxalases in bladder, kidney and testis cancers is reviewed.(GLO1, GLO2 (zeige HAGH Proteine))
Inhibition of GLO1 in Glioblastoma Multiforme Increases DNA-AGEs, Stimulates RAGE (zeige AGER Proteine) Expression, and Inhibits Brain Tumor Growth in Orthotopic Mouse Models
current research highlighted the Glo-I/AGE/RAGE (zeige AGER Proteine) system as an interesting therapeutic target in chronic liver diseases. These findings need further elucidation in preclinical and clinical studies.
GLO1-knockdown provoked collagen expression, endothelial inflammation and dysfunction and apoptosis which might contribute to vascular damage
Interdependence of GLO I and PKM2 in the Metabolic shift to escape apoptosis in GLO I-dependent cancer cells.
Induced Glyoxalase 1 expression is a common feature in the pathogenesis of oropharyngeal squamous cell carcinoma
The lowering of glycative stress via modulation of RAGE (zeige AGER Proteine)-AGE axis or glyoxalase 1 activity is beneficial for tubular homeostasis and the subsequent prevention and treatment of kidney disease, suggesting the possibility of novel therapeutic approaches which target glycative stress.
Glo-1 responds to dicarbonyl stress to enhance cytoprotection at the transcriptional level through stress-responsive increase of Glo-1 expression.
Transgenic mice overexpressing Glo1 on both FVB/NJ (FVB) or C57BL/6J (B6) backgrounds showed increased voluntary EtOH consumption compared to their wild-type littermates. Transgenic Glo1 knockdown mice on a B6 background showed decreased voluntary EtOH consumption. Genetic manipulations of Glo1 had no effect on sucrose, saccharin or water consumption.
the Glo1-methylglyoxal pathway integrates maternal and neural precursor cell metabolism to regulate neural development.
These data indicate that Glo1 knockout reduces anxiety-like behavior, but increases depression-like behavior.
Alternative detoxification of methylglyoxal in GLO1(-/-) is achieved by increased catalytic efficiency of aldose reductase (zeige AKR1B1 Proteine) toward hemithioacetal (product of glutathione and methylglyoxal ), which is most likely caused by S-nitrosylation of aldose reductase (zeige AKR1B1 Proteine).
Glo1 knockdown does not have major short term effects on the energy expenditure or the formation of atherosclerotic plaques.
Crystal structure of the mouse Glo1-inhibitor complex was determined at 2.3 A resolution.
Study demonstrates that GLO1 is a novel metabolic oncogene (zeige RAB1A Proteine) of the 6p21 amplicon, which promotes tumor growth and aberrant transcriptional signals via regulating cellular metabolic activities for energy production.
the balance between methylglyoxal and age-dependent GLO1 downregulation contributes to delayed wound healing in old mice
The difference in glyoxalase-1 mRNA was observed with Fkbp5 (zeige FKBP5 Proteine)-/- mice expressing 2-fold more glyoxylase-1 protein.
pharmacological inhibition of GLO1 reduced anxiety, suggesting that GLO1 is a possible target for the treatment of anxiety disorders.
The enzyme encoded by this gene is responsible for the catalysis and formation of S-lactoyl-glutathione from methylglyoxal condensation and reduced glutatione. Glyoxalase I is linked to HLA and is localized to 6p21.3-p21.1, between HLA and the centromere.
S-D-lactoylglutathione methylglyoxal lyase
, glx I
, glyoxalase domain containing 1
, ketone-aldehyde mutase
, lactoyl glutathione lyase
, lactoylglutathione lyase
, glyoxalase 1 complex
, glyoxalase 1 regulatory
, glyoxalase 1 structural
, glyoxalase I
, hypothetical protein
, trypanothione-dependent glyoxalase I
, glyoxylase 1