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Hu, Zhang, Tang, Su, Li, Chen, Zhang, Cai, Zhu: Variant G6PD levels promote tumor cell proliferation or apoptosis via the STAT3/5 pathway in the human melanoma xenograft mouse model. in BMC cancer 2013
Show all 6 Pubmed References
Human Glucose-6-Phosphate Dehydrogenase ELISA Kit for Sandwich ELISA - ABIN417357
Gabriel, Montevilla, Chida, Dias, Montoya, Otsubo, Pires, Nogaroto: Experimental research with synthetic copolymer-coated cardiopulmonary bypass circuits: inflammatory and thrombogenicity analysis. in Artificial organs 2012
We concluded that the MeltPro G6PD assay is useful as a diagnostic or screening tool for G6PD deficiency in clinical settings
The glucose-6-phosphate dehydrogenase enzymatic deficiency was significantly higher in males compared to females in Burkina Faso. (Review)
This work expands the current understanding of the biochemical underpinnings of G6PD variant pathogenicity.
This study assessed quantitatively the hemolytic risk with tafenoquine in female healthy volunteers heterozygous for the Mahidol(487A) glucose-6-phosphate dehydrogenase (G6PD)-deficient variant versus G6PD-normal females.
only in the case of G6PD and TALDO, the ratio of BrdU incorporation to DNA was significantly changed. The presented results together with our previously published studies illustrate the complexity of the influence of genes coding for central carbon metabolism on the control of DNA replication in human fibroblasts, and indicate which of them are especially important in this process.
Data suggest that G6PD PT materials can be stored at 4 degrees C and used for up to one month and can be stored at -20 degrees C for one year and yield >90% enzyme activity. Exposure to warm temperatures, especially with elevated humidity, should be avoided. Desiccant should always be used to mitigate humidity effects
We found that 2 G6PD variant genotypes were associated with elevated sTfR (show TFRC ELISA Kits) concentrations, which limits the accuracy of sTfR (show TFRC ELISA Kits) as a biomarker of iron status in this population.
immature reticulocytes (CD71 (show TFRC ELISA Kits)+) targeted by P. vivax invasion are enzymatically normal, even in hemizygous G6PD-Mahidol G487A mutants; thus, allowing the normal growth, development, and high parasite density in severely deficient samples
review of the state of the art in G6PD deficiency, describing 217 mutations in the g6pd gene; also compiled information about 31 new mutations, 16 that were not recognized and 15 more that have recently been reported; found that class I mutations have the most deleterious effects on the structure and stability of the protein
We now provide an additional evidence form Palestinian G6PD-deficient subjects for a possible role of 3' UTR (show UTS2R ELISA Kits) c.*+357 A>G, c.1365-13T>C, and/or c.1311C>T polymorphism for G6PD deficiency, suggesting that not only a single variation in the exonic or exonic intronic boundaries, but also a haplotype of G6PD should considered as a cause for G6PD deficiency.
higher (p<0.05) levels of G6PD were observed in SCNT deme and in vitro-derived groups in comparison to somatic cell nuclear transfer conv
Hyperthermia-induced Hsp90 (show HSP90 ELISA Kits).eNOS (show NOS3 ELISA Kits) preserves mitochondrial respiration in hyperglycemic endothelial cells by down-regulating Glut-1 (show SLC2A1 ELISA Kits) and up-regulating G6PD activity.
Glc-6-PD and NADPH redox are crucially involved in the mechanism of hypoxic pulmonary artery contraction and, in turn, may play a key role in increasing pulmonary arterial pressure
Levels of G6PD and HPRT (show HPRT1 ELISA Kits) RNA were higher in female morulae and blastocysts than in males, but only G6PD levels were significantly different between the sexes
Overexpression of G6PD in vascular endothelial cells decreases reactive oxygen species accumulation in response to exogenous and endogenous oxidant stress and improves levels of bioavailable NO.
In bovine retinal endothelial cells & pericytes, aldosterone reduced G6PD mRNA. A reduction in G6PD may be an early response to aldosterone.
Glucose 6-phosphate dehydrogenase is regulated through c-Src-mediated tyrosine phosphorylation in endothelial cells.
This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene.
, glucose-6-phosphate dehydrogenase, G6PD
, Glucose-6-phosphate 1-dehydrogenase
, glucose-6-phosphate 1-dehydrogenase (G6PD)
, glucose-6-phosphate dehydrogenase
, glucose-6-P dehydrogenase
, glucose-6-phosphate dehydrogenase X-linked
, glucose-6-phosphate dehydrogenase 2
, glucose dehydrogenase
, glucose oxidase
, glucose-6-phosphate 1-dehydrogenase 2
, glucose-6-phosphate dehydrogenase X-linked, pseudogene 1