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Rat (Rattus) SLC2A4 ELISA Kit for Sandwich ELISA - ABIN578069
Guo, Zhang, Li, Wang, Xiao, Yang: Hypoglycemic and hypolipidemic effects of oxymatrine in high-fat diet and streptozotocin-induced diabetic rats. in Phytomedicine : international journal of phytotherapy and phytopharmacology 2014
Dog (Canine) SLC2A4 ELISA Kit for Sandwich ELISA - ABIN649211
Schnurr, Reynolds, Gustafson, Duffy, Dunlap: Conditioning causes an increase in glucose transporter-4 levels in mononuclear cells in sled dogs. in The international journal of biochemistry & cell biology 2014
Mouse (Murine) SLC2A4 ELISA Kit for Sandwich ELISA - ABIN415677
Głombik, Stachowicz, Ślusarczyk, Trojan, Budziszewska, Suski, Kubera, Lasoń, Wędzony, Olszanecki, Basta-Kaim: Maternal stress predicts altered biogenesis and the profile of mitochondrial proteins in the frontal cortex and hippocampus of adult offspring rats. in Psychoneuroendocrinology 2015
Rat (Rattus) SLC2A4 ELISA Kit for Sandwich ELISA - ABIN431647
Ali, El-Abhar, Kamel, Attia: Antidiabetic Effect of Galantamine: Novel Effect for a Known Centrally Acting Drug. in PLoS ONE 2015
Rat (Rattus) SLC2A4 ELISA Kit for Sandwich ELISA - ABIN585388
Kamel, Helmy, Hanafi, Mahmoud, Abo Elfetooh: Impaired peripheral glucose sensing in F1 offspring of diabetic pregnancy. in Journal of physiology and biochemistry 2014
The results of the study confirmed the presence of GLUT-1 (show SLC2A1 ELISA Kits), GLUT-4 and GLUT-9 (show SLC2A6 ELISA Kits) proteins in the trophoblast from both, uncomplicated and diabetic pregnancies. In addition, insulin (show INS ELISA Kits) therapy may increase placental expression of GLUT-4 and GLUT-9 (show SLC2A6 ELISA Kits), and partially GLUT-1 (show SLC2A1 ELISA Kits), in women with pregestational and gestational diabetes mellitus.
our study has found that BMI, hypertension, myometrial invasion, pathological type, and Glut4 positive expression might be prognostic factors of EC [Endometrial cancer ]
Our work highlights the convenience and efficiency of this novel pH-sensitive fluorescent probe and reveals the new biological activity of staurosporine as an agonist for GLUT4 translocation and as an effective insulin (show INS ELISA Kits) additive analogue.
studies demonstrate that Elmo2 (show ELMO2 ELISA Kits) is a new regulator of insulin (show INS ELISA Kits)-dependent Glut4 membrane translocation through modulating Rac1 activity and Akt (show AKT1 ELISA Kits) membrane compartmentalization.
This review focuses on recent advances on the role of these signaling pathways and transcription factors involved in the regulation of CD36 (show CD36 ELISA Kits) and GLUT4.
effects of physiologically relevant phospholipids on glucose transport in liposomes containing purified GLUT4 and GLUT3 (show SLC2A3 ELISA Kits). The anionic phospholipids, phosphatidic acid, phosphatidylserine, phosphatidylglycerol, and phosphatidylinositol, were found to be essential for transporter function by activating it and stabilizing its structure.
These results suggest that the initial event caused by overnutrition may be oxidative stress, which produces insulin (show INS ELISA Kits) resistance, at least in part, via carbonylation and oxidation-induced inactivation of GLUT4.
A single bout of exercise elicited similar GLUT4 translocation in skeletal muscle of PCOS and Controls. The absence of impairment in GLUT4 translocation suggests that PCOS patients with obesity and insulin (show INS ELISA Kits) resistance may benefit from exercise training.
SLC2A4 gene expression level was slightly lower within type 2 diabetic patients in both type of tissues. Furthermore, the negative correlation between SLC2A4 gene expression level in visceral adipose tissue and BMI has been noticed
Leptin (show LEP ELISA Kits) at concentrations used in the study does not change glucose transport into lymphocytes and seems to have no influence on the expression of GLUT1 (show SLC2A1 ELISA Kits), GLUT3 (show SLC2A3 ELISA Kits), GLUT4 and and leptin (show LEP ELISA Kits) receptors
Feed intake remains low whereas respiratory frequency and body temperature remain higher and expression of HSP90 (show HSP90 ELISA Kits), CAT1 (show SLC7A1 ELISA Kits), SGLT1 (show SLC5A1 ELISA Kits) and GLUT4 increases in some tissues in pigs under chronic heat stress conditions.
TBC1D4, insulin receptor (show INSR ELISA Kits) and GLUT4 showed altered expression in some tissues in pre-diabetic pigs.
analysis of time- and breed-specific expression patterns of GLUT2 (show SLC2A2 ELISA Kits) and GLUT4, which highlight their potential as candidate genes for assessing adipose deposition and muscle development in pigs
Chronic elevated calcium blocks AMPK (show PRKAA1 ELISA Kits)-induced GLUT-4 expression in skeletal muscle.
Insulin (show INS ELISA Kits) resistance was associated with a significantly reduced total GLUT4 content in omental adipose tissue, without a change in content in other visceral or subcutaneous adipose sites.
There was a significant difference when pooled means for Glut-4 expression in muscle compared with adipose tissue from different anatomical sites.
E4-ORF1 (show MED14 ELISA Kits) activation of PI3K in adipocytes recapitulates insulin (show INS ELISA Kits) regulation of FoxO1 (show FOXO1 ELISA Kits) but not regulation of Glut4. This uncoupling of PI3K effects occurs despite E4-ORF1 (show MED14 ELISA Kits) activating PI3K and downstream signaling to levels achieved by insulin (show INS ELISA Kits).
Authors suggest that sortilin (show SORT1 ELISA Kits)- and retromer-mediated Glut4 retrieval from endosomes may represent a step in the Glut4 pathway vulnerable to the development of insulin (show INS ELISA Kits) resistance and diabetes.
It was concluded that ILK (show ILK ELISA Kits) depletion modifies the transcription of GLUT4, which results in reduced peripheral insulin (show INS ELISA Kits) sensitivity and glucose uptake, suggesting ILK (show ILK ELISA Kits) as a molecular target and a prognostic biomarker of insulin (show INS ELISA Kits) resistance.
Data, including data from studies using knockout/transgenic mice, suggest that PrPC (show PRNP ELISA Kits) is involved in development of insulin (show INS ELISA Kits) resistance and obesity; primary embryonic fibroblasts cultured from PrPC (show PRNP ELISA Kits) knockout mice exhibit reduced glucose uptake upon insulin (show INS ELISA Kits) stimulation due to reduced translocation of glucose transporter Glut4 to cell membrane. (PrPC (show PRNP ELISA Kits) = cellular prion protein (show PRNP ELISA Kits); Glut4 = facilitated glucose transporter (show SLC2A12 ELISA Kits) 4)
Our findings implicate Rac1 as a regulatory element critical for controlling glucose uptake during exercise via regulation of GLUT4 translocation.
insulin (show INS ELISA Kits) and insulin (show INS ELISA Kits) resistance regulate the spatial organization of GLUT4 in adipocytes.
these results indicate that PI3K and Akt ( Akt1 (show AKT1 ELISA Kits)-Akt3 (show AKT3 ELISA Kits))play distinct roles, and that PI3K stimulates Akt (show AKT1 ELISA Kits)-independent pathways that are important for GLUT4 translocation.
We confirmed that procyanidins suppressed acute hyperglycemia with an oral glucose tolerance test in a dose-dependent manner.procyanidins, especially cinnamtannin A2, significantly ameliorate postprandial hyperglycemia at least in part by promoting GLUT4 translocation to the plasma membrane by activating both insulin (show INS ELISA Kits)- and AMPK (show PRKAA1 ELISA Kits)-signaling pathways.
DHHC7 (show ZDHHC7 ELISA Kits) KO mice developed hyperglycemia and glucose intolerance, thereby confirming that DHHC7 (show ZDHHC7 ELISA Kits) represents the principal PAT for Glut4 and that this mechanism is essential for insulin (show INS ELISA Kits)-regulated glucose homeostasis
Brain GLUT4 knockout mice are glucose intolerant, insulin (show INS ELISA Kits) resistant, and have impaired glucose sensing, indicating a critical role for brain GLUT4 in sensing and responding to changes in blood glucose.
Low GLUT1 (show SLC2A1 ELISA Kits) and GLUT3 (show SLC2A3 ELISA Kits) expression in nonclassical monocytes was unaltered during differentiation into macrophages. GLUT4 mRNA was only detectable in unstimulated macrophages. Neither monocytes nor macrophages were insulin (show INS ELISA Kits) responsive.
Results of the present study suggest that myostatin (show MSTN ELISA Kits) inhibits the expression of GLUT4 mRNA and that the greater ability of double muscled cattle to produce muscle may be due to their greater sensitivity to insulin (show INS ELISA Kits) and greater use of glucose.
GLUT4 gene expression increased during late lactation.
These results suggest that goat GLUT4 functions in the transport of glucose and it may play a positive role in amino acid uptake in mammary glands.
This gene is a member of the solute carrier family 2 (facilitated glucose transporter) family and encodes a protein that functions as an insulin-regulated facilitative glucose transporter. In the absence of insulin, this integral membrane protein is sequestered within the cells of muscle and adipose tissue. Within minutes of insulin stimulation, the protein moves to the cell surface and begins to transport glucose across the cell membrane. Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM).
, glucose transporter type 4, insulin-responsive
, insulin-responsive glucose transporter type 4
, solute carrier family 2, facilitated glucose transporter member 4
, glucose transporter 4
, glucose transporter type 4
, solute carrier family 2 (facilitated glucose transporter), member 4
, solute carrier family 2, facilitated glucose transporter member 4-like
, Insulin-responsive glucose transporter
, insulin-responsive glucose transporter 4
, insulin-responsive glucose transporter
, Glucose transporter 4 insuline-responsive
, Glucose transporter 4, insuline-responsive
, solute carrier family 2 member 4
, solute carrier family 2 , member 4